Diabeta (Glyburide)

Author , posted on June 20, 2017

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Diabeta

Glyburide (Glibencamide)

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Glyburide (Generic)

Glyburide (Glibencamide)

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Diabeta (Glyburide) Dosage and Side Effects

DIABETA is used along with diet and exercise to help control blood-sugar levels in people who have type 2 diabetes. DIABETA is in a class of drugs known as sulfonylureas, which stimulate the pancreas to produce the hormone insulin.

Warnings and Precautions

You shouldn't take DIABETA if you have type 1 diabetes (the body doesn't produce any insulin) or diabetic ketoacidosis (a dangerous condition that can occur if high blood sugar is untreated).

Before taking this medicine, tell your doctor if you have or have ever had:

  • G6PD deficiency (an inherited enzyme condition)
  • Hemolytic anemia (a lack of red blood cells)
  • Hormone disorders involving the pituitary, adrenal, or thyroid gland
  • Heart, kidney, or liver disease
  • A nerve disorder that affects bodily functions

Alert your physician if you've taken chlorpropamide (Diabenese), another sulfonylurea drug for diabetes, in the past two weeks.

You shouldn't take this medicine if you take bosentan (Tracleer), a drug used for high blood pressure in the lungs (pulmonary arterial hypertension), because it may increase your risk of liver problems.

Before having surgery, including a dental procedure, tell your doctor or dentist that you are taking DIABETA.

Some diabetes drugs may increase your risk of serious heart problems.  However, blood sugars that are out of control can damage your heart, or other organs, too. Talk to your doctor about these risks.

Tell your physician if you experience an illness, fever, injury, or unusual stress while taking DIABETA, because these can change your blood sugar and the dosage you need. DIABETA may cause changes in your blood sugar.

You should know the symptoms of high (hyperglycemic) or low (hypoglycemic) blood-sugar episodes and be prepared to treat them.

Your doctor will probably want to check your glucose levels often while you are taking DIABETA. Keep all healthcare appointments, including the ones for tests at a lab.

This medicine helps control blood-sugar levels, but it doesn't cure diabetes. Don't stop taking DIABETA without first talking to your doctor.  Always wear a diabetic ID bracelet to be sure you get proper treatment in case of an emergency.

Pregnancy and DIABETA

DIABETA is a pregnancy category C drug, which means harm to an unborn baby can't be ruled out.  Tell your physician if you are, or if you are planning, to become pregnant. Your healthcare provider might want you to take insulin during pregnancy.

Don't breastfeed while using this drug. It's not known whether DIABETA passes into breast milk or could harm a breastfeeding baby.

Gestational Diabetes and DIABETA

DIABETA is sometimes used to treat women with a form of diabetes that occurs during pregnancy (known as gestational diabetes).  However, some studies have found DIABETA may not be as safe or as effective as injected insulin.  Other studies have shown women with gestational diabetes may need higher doses of DIABETA. Talk to your doctor about the potential risks and benefits of using this medicine to treat gestational diabetes.

Side Effects

Common Side Effects of DIABETA

Tell your doctor if any of the following side effects become severe or don't go away:

  • Heartburn
  • Nausea
  • Upper abdominal fullness
  • Rash
  • Muscle or joint pain
  • Blurred vision

Serious Side Effects of DIABETA

Call your doctor immediately if you experience any of the following serious side effects:

  • Dark urine
  • Light-colored stools
  • Yellowing of the eyes or skin (jaundice)
  • Fever
  • Sore throat
  • Diarrhea

If you have any of the following and can't reach your doctor, you may need emergency medical help:

  • Pain in the upper right portion of the stomach
  • Confusion or slurred speech
  • Severe weakness
  • Unusual bleeding or bruising
  • Swelling of the eyes, face, lips, tongue, or throat

Interactions with this medication

Tell your doctor about all prescription, non-prescription, illegal, recreational, herbal, nutritional, or dietary drugs you're taking, especially:

  • Angiotensin-converting enzyme (ACE) inhibitors, such as benazepril (Lotensin), captopril (Capoten), enalapril (Vasotec), fosinopril (Monopril), lisinopril (Prinivil, Zestril), moexipril (Univasc), perindopril, (Aceon), quinapril (Accupril), ramipril (Altace), and trandolapril (Mavik)
  • Antibiotics known as quinolone or fluoroquinolone, such as cinoxacin (Cinobac), ciprofloxacin (Cipro), enoxacin (Penetrex), gatifloxacin (Tequin), levofloxacin (Levaquin), lomefloxacin (Maxaquin), moxifloxacin (Avelox), nalidixic acid (NegGram), norfloxacin (Noroxin), ofloxacin (Floxin), sparfloxacin (Zagam), or trovafloxacin and alatrofloxacin combination (Trovan)
  • Aspirin and other nonsteroidal anti-inflammatory medications (NSAIDs), such as ibuprofen (Advil, Motrin) and naproxen (Aleve, Naprosyn)
  • Asthma drugs
  • Blood thinners, such as warfarin (Coumadin)
  • Beta blockers, such as atenolol (Tenormin), labetalol (Normodyne), metoprolol (Lopressor, Toprol XL), nadolol (Corgard), and propranolol (Inderal)
  • Bosentan (Tracleer), for high blood pressure in the lungs (pulmonary hypertension)
  • Calcium channel blockers, such as amlodipine (Norvasc), diltiazem (Cardizem, Dilacor, Tiazac, others), felodipine (Plendil), isradipine (DynaCirc), nicardipine (Cardene), nifedipine (Adalat, Procardia), nimodipine (Nimotop), nisoldipine (Sular), and verapamil (Calan, Isoptin, Verelan)
  • Chloramphenicol, an antibiotic
  • Clarithromycin (Biaxin), an antibiotic
  • Cold medicines
  • Contraceptives, such as birth control pills, patches, rings, implants, and injections
  • Cyclosporine (Neoral, Sandimmune), an immunosuppressant
  • Diabetes and blood-sugar drugs, such as insulin and others
  • Disopyramide (Norpace), a heart drug
  • Fluconazole (Diflucan), for fungal infections
  • Hormone replacement therapy
  • Isoniazid (INH)
  • MAOIs, such as isocarboxazid (Marplan), phenelzine (Nardil), selegiline (Eldepryl, Emsam, Zelapar), and tranylcypromine (Parnate)
  • Mental illness medications, such as fluoxetine (Prozac, Sarafem) and others
  • Miconazole (Monistat), for yeast infections
  • Nausea medicine
  • Niacin, a type of vitamin B used for many conditions
  • Oral steroids such as dexamethasone (Decadron, Dexone), methylprednisolone (Medrol), and prednisone (Deltasone)
  • Phenytoin (Dilantin), a seizure medicine
  • Probenecid (Benemid), for preventing gout or to treat some types of arthritis
  • Rifampin, an antibiotic for tuberculosis
  • Salicylate pain relievers such as choline magnesium trisalicylate, choline salicylate (Arthropan), diflunisal (Dolobid), magnesium salicylate (Doan's, others), and salsalate (Argesic, Disalcid, Salgesic)
  • Sulfa drugs, including antibiotics, such as co-trimoxazole (Bactrim, Septra); and the arthritis drug sulfasalazine (Azulfidine)
  • Thyroid medications
  • Water pills (diuretics)

If you take colesevelam (Welchol), a drug for lowering "bad" (LDL) cholesterol, don't take it until four hours after you've taken DIABETA.

Avoid drinking alcohol while taking DIABETA, as it can lower blood sugar and increase your risk of side effects.Although rare, drinking alcoholic beverages while on DIABETA can cause headache, flushing, nausea, vomiting, chest pain, weakness, blurred vision, sweating, choking, mental confusion, breathing difficulties, or anxiety.

DIABETA can make your skin more sensitive to sunlight. Avoid unnecessary sun exposure and tanning beds. Also, wear protective clothing and sunscreen when you are outdoors.

This medicine may also make you drowsy or dizzy. Don't drive or perform any activity that requires alertness until you're sure you can do so safely.

Proper Use of this medication

This medicine is usually taken once a day. However, some people may take it twice a day. Follow the directions carefully when taking DIABETA. Don't take more or less of the drug than is prescribed.  Your doctor might start you on a low dose and gradually increase it if needed.

If you suspect an overdose, you should contact a poison-control center or emergency room immediately.

Ask your doctor what to do if you forget a dose of DIABETA, and write down those instructions. As a general rule, if you miss a dose, take it as soon as your remember.

However, if it's almost time for your next dose, skip the missed dose and continue on your regular dosing schedule.  Don't take extra medicine to make up for a missed dose.

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Ridaura (Auranofin)

Author , posted on June 20, 2017

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Ridaura

Auranofin

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Ridaura (Auranofin) Dosage and Side Effects

RIDAURA is used to treat rheumatoid arthritis. RIDAURA is a form of gold that reduces some of the effects of the inflammatory process in the body.

Warnings and Precautions

You should not use this medication if you have ever had a severe reaction to gold therapy that affected your skin, lungs, bone marrow, blood cells, or your stomach or intestines.

Before taking RIDAURA, tell your doctor if you have a weak immune system, bone marrow disorder, kidney or liver disease, or inflammatory bowel disease.

RIDAURA can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. To be sure your blood cells do not get too low, your blood will need to be tested on a regular basis.

Keep using RIDAURA as directed. Talk with your doctor if your symptoms do not improve after 3 or 4 months of treatment.

Stop taking RIDAURA and call your doctor at once if you have a skin rash or itching, mouth sores, severe diarrhea, easy bruising or bleeding, blood in your urine or stools, coughing up blood, or unusual weakness, or any signs of infection (fever, chills, flu symptoms).

You should not use this medication if you are allergic to RIDAURA, or if you have ever had any of these medical problems caused by using gold therapy:

  • an allergic skin reaction;
  • stomach or intestinal problems;
  • a breathing disorder;
  • a bone marrow disorder; or
  • a severe blood cell disorder.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely use this medication:

  • a bone marrow disorder or weak immune system;
  • kidney disease;
  • liver disease; or
  • inflammatory bowel disease.

FDA pregnancy category C. It is not known whether RIDAURA is harmful to an unborn baby. Before taking this medication, tell your doctor if you are pregnant or plan to become pregnant during treatment.

It is not known whether RIDAURA passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Side Effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Stop taking this medication and call your doctor at once if you have a serious side effect such as:

  • itching or skin rash;
  • white patches or sores inside your mouth or on your lips;
  • pain or swelling in your gums or tongue, metallic taste in your mouth;
  • severe or ongoing diarrhea;
  • severe nausea, vomiting, stomach cramps;
  • pale skin, easy bruising or bleeding;
  • blood in your urine;
  • weakness or fainting;
  • black, bloody, or tarry stools; or
  • coughing up blood or vomit that looks like coffee grounds.

Less serious side effects may include:

  • mild stomach pain or upset;
  • gas, bloating; or
  • loss of appetite.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Interactions with this medication

Avoid being near people who have colds, the flu, or other contagious illnesses. Contact your doctor at once if you develop signs of infection.

Avoid exposure to sunlight, sunlamps, or tanning beds. RIDAURA can make your skin more sensitive to sunlight, and a sunburn may result. Wear protective clothing and use sunscreen (SPF 15 or higher) when you are outdoors.

Tell your doctor about all other medications you use, especially:

  • gold injections;
  • hydroxychloroquine (Plaquenil);
  • penicillamine (Cuprimine, Depen);
  • phenytoin (Dilantin);
  • high doses of steroid medication (prednisone and others); or
  • drugs that weaken your immune system, such as cyclophosphamide (Cytoxan, Neosar), azathioprine, methotrexate (Rheumatrex, Trexall), and others.

This list is not complete and there may be other drugs that can interact with RIDAURA. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.

Proper Use of this medication

Take this medication exactly as prescribed by your doctor. Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Your doctor may occasionally change your dose to make sure you get the best results from this medication.

Take this medicine with a full glass of water.

RIDAURA can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. To be sure your blood cells do not get too low, your blood will need to be tested on a regular basis. Do not miss any scheduled appointments.

Contact your doctor at once if you develop signs of infection such as fever, chills, sore throat, flu symptoms, easy bruising or bleeding (nosebleeds, bleeding gums), loss of appetite, nausea and vomiting, mouth sores, or unusual weakness.

It may take up to 6 months of using this medicine before your symptoms improve. For best results, keep using the medication as directed. Talk with your doctor if your symptoms do not improve after 3 or 4 months of treatment.

Store RIDAURA at room temperature away from moisture, heat, and light.

Seek emergency medical attention if you think you have used too much of this medicine.

Symptoms of an RIDAURA overdose are not known.

Take the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to take the medicine and skip the missed dose. Do not take extra medicine to make up the missed dose.

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Uceris (Budesonide)

Author , posted on June 20, 2017

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Uceris

Budesonide

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Uceris

Budesonide

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Check Uceris (Budesonide) Cost Online with PricePro Pharmacy

Uceris is a prescription medication. It is taken mainly by those who have the Crohn’s disease of the intestines. If you want to find out how to buy Uceris online, call PricePro Pharmacy customer care or simply follow our "How to Order" guide. We are also available for live chat and we can answer your questions in terms of how to send your prescription or how long it will it take to receive your order.

Uceris is manufactured by Cosmo Pharmaceuticals and Ferring Inc. and available in a 9mg extended-release tablet. We offer this medication from Canada and New Zealand with an alternative name called Cortiment, with an estimated shipping time of 7-10 business days from Canada and 10-18 business days from New Zealand. Uceris is packaged in boxes of 30 tablets per pack.   To view our low price Uceris medicine and more, click on the dosage box shown above.

Uceris (Budesonide) Medication Information

Uses

Your healthcare provider may prescribe Uceris for the treatment of active ulcerative colitis (UC). Uceris is indicated to induce remission in those experiencing mild to moderate UC.

Common symptoms of UC include diarrhea, stomach pain, weight loss, fatigue, constipation, and rectal bleeding. The condition is chronic, and patients experience acute “flares” that can be treated to remission. Once in remission, different medications are used to maintain remission.

The cause of UC is not fully understood, but it is likely related to a combination of environmental and genetic factors. The symptoms of UC are caused by the immune system becoming too active in the large intestine. The lining of the large intestine becomes swollen and inflamed.

Uceris is a glucocorticoid, which is a type of steroid that decreases the activity of the immune system. Uceris is not absorbed into the bloodstream, and it works directly on the inflamed cells of the large intestine. By decreasing inflammation, UC is put into remission, and the symptoms resolve.

Dosage

The usual dosage of Uceris is 9 mg by mouth once daily for up to eight weeks. Take Uceris exactly as prescribed by your doctor. Your length of treatment will vary based on the severity of your condition.

Uceris can be taken with or without food.

Side Effects

Common side effects of Uceris may include:

  • Abdominal distension
  • Acne vulgaris
  • Arthralgia
  • Bruise
  • Constipation
  • Decreased cortisol
  • Flatulence
  • Headache
  • Moon face
  • Nausea
  • Respiratory tract infection
  • Upper abdominal pain
  • Urinary tract infection

Precautions

Tell your doctor if you have a history of chronic infection, including viral, bacterial, fungal, or other. Uceris and other glucocorticoids can increase the risk of symptom recurrence.

Long-term use of systemic glucocorticoids can lead to hypercorticism and adrenal suppression. The risk is generally lower with Uceris than other glucocorticoids because it does not absorb well into the bloodstream. However, ask your doctor or pharmacist to review hypercorticism and adrenal suppression.

Interactions

Common drug-drug interactions include:

  • Atazanavir
  • Ceritinib
  • Clarithromycin
  • Cobicistat and cobicistat-containing coformulations
  • Darunavir
  • Grapefruit juice
  • Indinavir
  • Itraconazole
  • Ketoconazole
  • Lopinavir
  • Mifepristone
  • Nefazodone
  • Nelfinavir
  • Ombitasvir-paritaprevir-ritonavir
  • Ombitasvir-paritaprevir-ritonavir plus dasabuvir
  • Posaconazole
  • Ritonavir and ritonavir-containing coformulations
  • Saquinavir
  • Telithromycin
  • Tucatinib
  • Voriconazole

Tell your doctor and pharmacist about all medications you are taking, including over-the-counter, herbal medicines, and supplements.

Storage

Store near room temperature at 25°C (77°F). 

Pharmacist Tips

  • Uceris is taken for up to eight weeks at a time until UC has gone into remission. Once remission is achieved, you will be switched to a different medication to maintain remission.
  • Protect Uceris from light and moisture.
  • Do not break, crush, or chew Uceris. Swallow them whole with water.

Uceris FAQs

What time of day should I take Uceris?

Uceris is best taken in the morning.

 

What if I miss a dose of my medication?

If if it is within a few hours of your normal dosage time, take it as soon as you remember. However, if it is almost time for your next dose, skip the missed dose. Do not double up.

 

How will I know if Uceris is working?

You should notice a reduction in UC symptoms within 3-7 days.

 

Related Products

References

  1. Uceris [package insert]. San Diego, CA: Santarus; 2013.

Medication Review by a Clinical Pharmacist - PharmD

Author: Dr. Conor Sheehy, PharmD, BCPS

Dr. Sheehy is a board-certified pharmacotherapy specialist. He has worked in multiple practice settings, including retail and hospital pharmacies, and in medical clinics.  He specializes in anticoagulation, psychiatric medications, and diabetes medications. He strives to empower his patients to understand their medications and improve their overall medical care.

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Acular LS Eye Drops (Ketorolac)

Author , posted on June 20, 2017

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Acular LS Eye Drops

Ketorolac Tromethamine

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Buy Acular LS Online

To order your Acular LS prescription online you can call toll-free at 1-855-776-0079 or navigate our website and order online.

You can click on the "CHECK PRICES" dosage box above to view more product details.

Please note that a prescription is required to purchase medication from our online pharmacy. The prescription can be emailed, faxed, or uploaded by "Rx Upload" feature on your laptop or mobile device.

Acular LS Price Comparison Between USA and Canada

The average retail price of 5 ml(s) of Acular LS 0.4% in the United States is:

  • $280.00 for 1 eye drop bottle

At PricePro Pharmacy the price is as low as:

  • $36.00 for 1 eye drop bottle

You can save up to 87% when you order this medication online from our trusted service. Our low cost is without any insurance assistance or Acular coupons.

Available Products

The following dosage is available to order:

  • 0.4%

We only carry the brand product made by Allergan available in 5 mL eye drop pack size. There is no generic Acular LS available to purchase with our online pharmacy.

The active medicinal ingredient found in Acular LS is ketorolac.

Delivery Times

Two options are available to order from with different shipping times. The product dispensed from our partner pharmacy in Canada will take 7-10 business days to ship to USA while the product of India will take 10-18 business days.

When you order ships from the dispensing pharmacy you will be notified by an email alert with applicable tracking information if tracked shipping is selected.

There is a standard shipping charge of $9.95 per order.

Acular LS Prescription Refill

Take advantage of our friendly refill reminder service to ensure that you won't run out of supply of your medication. We can update you by an email or phone call reminder when you should be placing a refill order based on your prescription history.

You can also log into your online account to place a re-order online based on your previous order history.

Acular LS Eye Drops (Ketorolac) Product Information

Acular LS Eye Drops is a NSAID medication for reducing eye itching triggered by seasonal allergies. It can also be used in after-care post cataract or corneal refractive surgery, to relieve swelling, pain, or burning.

What is Acular LS Eye Drop Prescribed for?

The active ingredient for this medication is called Ketorolac. It is a non-steroidal anti-inflammatory drug or NSAID for minimizing body chemicals that trigger pain and inflammation. It is specifically designed for eye irritation due to seasonal allergies. It comes in the form of eye drops and is able to reduce swelling, pain, burning and stinging that results from surgery— cataracts or corneal refractive surgeries. This eye drop can also be prescribed for any other condition your doctor prefers.

Directions

If your doctor has decided that you are going to use this medicine, it is good to know how to do this. First of all, never take a smaller or a larger dose than needed. Next, Use your medication two times to four times every day. If your doctor’s prescription is specific, follow it to the letter.  Moreover, stop using once the period recommended by the doctor comes to an end. That’s because prolonged use of NSAID eye drops can harm your vision.

If you want to avoid irritation that may emerge after doing cataracts surgery, use the medication a day prior to the procedure. Then continue to use it for two weeks after surgery. If undergoing corneal refractive surgery, use this medication four times daily for up to four days after the procedure.  In case you are going to have surgery in one eye, use the medicine there only. If you wear contact lenses, stop when using this eye drop medicine. The process of application is simple.

First tilt your head back and pull down your lower eyelid. A tiny pocket will form. Then, hold the dropper tip right above this eye, look up and away from the tip and squeeze out one drop of Acular LS. Close your eyes for two to three minutes while looking down. Don’t blink or squint. Instead, press your finger to the inner corner of your eye for a minute or two to allow the medication to drain into the tear duct.

If you have different eye drops products too, wait ten minutes utmost before using them. Make sure that your eye drops are safe to use, that is they have not expired. As each bottle or vial is for one use only, throw yours way after one use. Discard it even if there is some medicine left.

Side Effects

Stop using if you already know that you have an allergy to Ketorolac. This will reduce your odds of having side effects. However, if you encounter side effects, they will be the types that affect every other user. These common side effects of Acular LS include:

  • Watery eyes
  • Swollen eyelids
  • Headache
  • Blurred vision
  • Mild pain in the eye
  • Stinging
  • Redness

These can go away in a short while and shouldn’t cause fear. If they persistent you should talk to your eye doctor. Additionally, if you notice other symptoms, such as severe eye pain, redness, vision changes, sensitivity to light and drainage from the eyes; make an appointment with your doctor.

Precautions

Prior to using this medication, ensure that you have a discussion with your eye doctor concerning your overall health. So, let them know that you are allergic to Ketorolac or other NSAIDS. Also, inform them about:

  • Arthritis
  • Glaucoma
  • Dry eye syndrome
  • Diabetes
  • A health condition for which you take a blood thinning drug like warfarin
  • A blood clotting disorder

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Desyrel (Trazodone)

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Desyrel

Trazodone Hydrochloride

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Trazodone (Generic)

Trazodone Hydrochloride

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Trazodone (Generic)

Trazodone Hydrochloride

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Trazodone HCl (Generic)

Trazodone Hydrochloride

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Desyrel (Trazodone) Dosage and Side Effects

DESYREL is an antidepressant drug that's prescribed to treat the symptoms of depression. Besides treating depression, doctors may also prescribe DESYREL  to treat anxiety, schizophrenia, or uncontrolled movements that occur as a side effect of other medications.  Your doctor may prescribe DESYREL to treat insomnia or other sleep disorders.

Warnings and Precautions

The risk of suicide is greatest when starting treatment or when increasing or decreasing the dose of DESYREL.  Suicide risk may be higher for people younger than 24.

Depression may become worse before it gets better when someone starts taking DESYREL.

Your doctor will watch you carefully for symptoms of aggression, irritability, panic attacks, extreme worry, restlessness, acting without thinking, abnormal excitement, or any thoughts of suicide when you start the drug. You should also let friends and family members know if you have these symptoms or worsening symptoms of depression.  If you have any thoughts of suicide or if a friend or family member thinks you are acting strangely, call a doctor right away.

Stopping DESYREL suddenly can cause withdrawal symptoms that include anxiety, agitation, and difficulty sleeping.

Children or teens should not take DESYREL.

Tell your doctor if you have:

  • Heart problems
  • Low orhigh blood pressure 
  • History of substance abuse
  • Any mental health disorders
  • Cancer
  • Anemia
  • Liver problems
  • Kidney problems
  • Diarrhea or vomiting

Anyone taking the drug should let their doctor know about any family history of suicide.

If you are a man, let your doctor know if you have any problem with an erection that will not go away (priapism).

It's important to tell your doctor if you have symptoms of aggression, irritability, panic attacks, extreme worry, restlessness, acting without thinking, abnormal excitement, or any thoughts of suicide while on DESYREL.

DESYREL 'High' and Abuse

Because DESYREL isn't regulated as strictly as other sleep medications, it has some potential for abuse by people seeking a high.  The drug has been anecdotally linked to hallucinations in high doses, but the risks of overdose and severe side effects make this a very dangerous recreational drug.

Take DESYREL only as directed, and keep this and all other drugs away from children, teenagers, and anyone for whom the drug has not been prescribed.

Pregnancy and DESYREL

DESYREL may cause harm to a developing fetus.  Some animal studies have found evidence of developmental abnormalities in fetuses that were exposed to the drug.

It's not known if DESYREL is safe for breastfeeding infants.  You should speak to your doctor about using DESYREL before breastfeeding, and if you are or might be pregnant.

Side Effects

Common side effects of DESYREL include:

  • Headache
  • Muscle ache
  • Nausea, vomiting, loss of appetite, or stomachache
  • Constipation or diarrhea
  • Loss of interest in sex (erectile dysfunction in men)
  • Dizziness or loss of balance
  • Dry mouth or dry eyes
  • Numbness, burning, or tingling sensations
  • Confusion
  • Blurred vision
  • Ringing in the ears
  • Nervousness or confusion
  • Rash
  • Sweating
  • Weakness or fatigue

Serious side effects can occur. If you have any of these side effects, stop taking DESYREL and call your doctor right away:

  • Worsening depression
  • Suicidal thoughts
  • A severe rash or hives
  • Swelling of the face, lips, or tongue
  • Chest pain
  • Difficulty breathing
  • A painful erection that will not go away (priapism)
  • Panic attack
  • Irregular heartbeat
  • Fainting
  • Unusual bruising or bleeding
  • Seizure

DESYREL also might cause some people to have auditory hallucinations while taking the drug.  However, evidence of this is preliminary and needs further investigation.

Interactions with this medication

It's very important to let your doctor know about all drugs you are taking, including illegal drugs and any over-the-counter (OTC) herbs or supplements.

Types of drugs that are known to interact with DESYREL include:

  • Blood thinners, including warfarin (Coumadin), aspirin, and ibuprofen
  • Drugs used to treat mental illness, including thioridazine; selective serotonin reuptake inhibitors (SSRIs), such as fluoxetine (Prozac, Sarafem) and fluvoxamine (Luvox); and MAOIs such as isocarboxazid (Marplan) and phenelzine (Nardil)
  • Diuretics
  • Cold, cough, and allergy medications, including dexamethasone (Decadron)
  • Medications used to treat fungal diseases, such as ketoconazole (Nizoral), itraconazole (Sporanox), and (Vfend)
  • Medications used to treat HIV/AIDS, including atazanavir (Reyataz), indinavir (Crixivan), and nelfinavir (Viracept)
  • Medications used to treat heartburn, including cimetidine (Tagamet) and cisapride (Propulsid)
  • Some antibiotics, such as clarithromycin (Biaxin, in Prevpac) and erythromycin (E.E.S., E-Mycin, Erythrocin)
  • Some heart medications, including sotalol (Betapace, Betapace AF) and verapamil (Calan, Isoptin, Verelan)
  • Some seizure medications, such as carbamazepine (Tegretol), ethosuximide (Zarontin), phenobarbital (Luminal, Solfoton), and phenytoin (Dilantin)

DESYREL may make you feel drowsy and may affect your judgment.  Until you know how DESYREL will affect you, don't drive or operate machinery.

Drinking alcohol may make some side effects of DESYREL more severe and cause problems.

Proper Use of this medication

Do not crush, snort, or chew a tablet.

Your doctor will start you on a low dose of DESYREL and increase the dose every three to four days.  It may take up to two weeks before you notice a response. A daily dose of DESYREL may range from 150 to 375 milligrams.

Take regular tablets two or more times a day with food.

If your doctor prescribes an extended-release tablet, you'll take it once a day at bedtime on an empty stomach.

DESYREL Overdose

Symptoms of a DESYREL overdose may include:

  • Vomiting
  • Drowsiness
  • Painful erection
  • Abnormal heartbeat
  • Trouble breathing
  • Seizures

If someone collapses or isn't breathing, call 9-1-1 immediately.

Missed Dose of DESYREL

Take DESYREL exactly as directed by your doctor.  Don't stop taking DESYREL on your own because stopping suddenly can cause withdrawal symptoms that include anxiety, agitation, and difficulty sleeping.

If you miss a dose of DESYREL, take the missed dose as soon as you remember. If it's almost time for your next dose, skip the missed dose.  Don't double your dose to make up for a missed dose.

Other related products

Onbrez Breezhaler (Indacaterol)

Author , posted on June 20, 2017

Category:


Onbrez Breezhaler

Indacaterol Maleate

Select Quantity:
Select Quantity:

Onbrez Breezhaler

Indacaterol Maleate

Select Quantity:
Select Quantity:

Onbrez Breezhaler (Indacaterol) Dosage and Side Effects

ONBREZ BREEZHALER is used to make breathing easier for people who have breathing difficulties due to a lung disease called chronic obstructive pulmonary disease (COPD).

Warnings and Precautions

Serious Warnings and Precautions

ONBREZ BREEZHALER should only be used to treat COPD.

You are advised that in patients with asthma, long-acting beta2-agonist (LABA) medicines, may increase the chance of death from asthma problems. In a large asthma study, more patients who used another LABA medicine (salmeterol) died from asthma problems compared with patients who did not use that LABA medicine. This finding may also apply to ONBREZ BREEZHALER.

BEFORE you use ONBREZ BREEZHALER talk to your doctor or pharmacist if you:

  • have heart problems, such as rapid or irregular heart beat or abnormal electrical signal called “prolongation of the QT interval”
  • have high blood pressure
  • have epilepsy
  • have thyroid gland problems
  • have diabetes
  • are pregnant or planning to become pregnant. It is not known if ONBREZ BREEZHALER may affect your unborn baby
  • are breastfeeding. It is not known if ONBREZ BREEZHALER passes into your milk and if it can affect your baby
  • are taking certain medications
  • ONBREZ BREEZHALER contains lactose (milk sugar) and a small amount of milk proteins. It is possible that allergic reactions may happen in patients who have a severe milk protein allergy.

During the treatment with ONBREZ BREEZHALER, tell your doctor immediately if you experience any of the following symptoms:

  • If you experience a tightness of the chest, coughing, wheezing or breathlessness immediately after inhalation (signs of bronchospasm)
  • If you experience difficulties in breathing or swallowing, swelling of tongue, lips and face, hives or itching, skin rash (signs of hypersensitivity reaction). Do not use ONBREZ BREEZHALER again before speaking with your doctor.
  • If your COPD symptoms (breathlessness, wheezing, cough) do not improve or if they worsen during your treatment

ONBREZ BREEZHALER does not relieve sudden symptoms of COPD. Always have a short-acting bronchodilator medicine with you to treat acute symptoms. If you do not have an inhaled, short-acting bronchodilator, contact your healthcare provider to have one prescribed for you.

Get emergency medical care if:

  • breathing problems worsen quickly
  • you use your short-acting bronchodilator medicine, but it does not relieve your breathing problems

Side Effects

Like all medicines, ONBREZ BREEZHALER can cause side effects in some people.

Some people occasionally cough soon after inhaling the medicine. If you do, don't worry, as long as the capsule is empty, you have received the full dose.

Common side effects include:

  • Nausea
  • Upper respiratory tract infections
  • Muscle cramp
  • Headache
  • Cough
  • Irritation of the mouth or throat

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

Interactions with this medication

Tell your doctor or a pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. This includes in particular the following medicines:

  • medicines used in the treatment of depression or sad mood (e.g. tricyclic antidepressants, monoamine oxidase inhibitors)
  • medicines similar to ONBREZ BREEZHALER (other LABA) used for your lung disease as it may increase the risk of experiencing possible side effects
  • medicines that decrease the level of potassium in your blood. These include diuretics (also known as “water pills” and used to treat hypertension e.g. hydrochlorothiazide), other bronchodilators such as methylxanthines (e.g. theophylline) or steroids (e.g. prednisolone)
  • beta-blockers used in the treatment of hypertension or other cardiac problems (e.g. propranolol) or in the treatment of glaucoma (e.g. timolol)

Proper Use of this medication

Follow your doctor's instructions carefully. Do not exceed the recommended dose.

Usual adult dose:

Inhale the contents of one capsule through the mouth each day, everyday at the same time, using the ONBREZ BREEZHALER inhalation device, even when you have no breathing problems or other symptoms of COPD.

You may inhale this medication in a fasting state or after food or drink.

How to inhale ONBREZ BREEZHALER:

Follow the instructions below. You will breathe in (inhale) the medicine in the ONBREZ BREEZHALER capsules from the ONBREZBREEZHALER inhalation device. If you have any questions, ask your healthcare provider or pharmacist.

The ONBREZ BREEZHALER package contains ONBREZ BREEZHALER capsules and one ONBREZ BREEZHALER inhalation device.

  • The ONBREZ BREEZHALER capsules are supplied in one or more blister cards. Each blister card contains 10 transparent capsules.
  • The ONBREZ BREEZHALER inhalation device consists of a cap and a base.

Your inhalation device is designed to deliver the medicine contained in the capsules. Do not use ONBREZ BREEZHALER capsules with any other capsule inhalation device, and do not use the ONBREZ BREEZHALER inhalation device to take any other capsule medicine.

  1. Pull off the cap
  2. Open inhalation device:
  3. Hold the base of the ONBREZ BREEZHALER inhalation device firmly and tilt the mouthpiece to open the inhalation device.
  4. Prepare capsule:
  5. Immediately before use, with dry hands, remove one capsule from the blister.
  6. Insert capsule:
  7. Place the capsule into the capsule chamber.
  8. Never place a capsule directly into the mouthpiece.
  9. Close the inhalation device:
  10. Close the inhalation device fully. You should hear a ‘click' as it fully closes.
  11. Pierce the capsule:
  12. Hold the inhalation device upright with the mouthpiece pointing up. Press both buttons fully one time. You should hear a ‘click' as the capsule is being pierced. Do not press the piercing buttons more than once.
  13. Release the buttons fully.
  14. Breathe out:
  15. Before placing the mouthpiece in your mouth, breathe out fully.
  16. Never blow into the mouthpiece.
  17. Inhale the medicine:
  18. Before breathing in, place the mouthpiece in your mouth and close your lips firmly around the mouthpiece. Hold the inhalation device with the buttons to the left and right (not up and down). Breathe in rapidly but steadily, as deeply as you can. Do not press the piercing buttons.
  19. Note:
  20. As you breathe in through the inhalation device, the capsule spins around in the chamber and you should hear a whirring noise. You will experience a sweet taste as the medicine goes into your lungs. If you do not hear a whirring noise, the capsule may be stuck in the capsule cavity. If this occurs, open the inhalation device and carefully loosen the capsule by tapping the base of the device. Do not press the piercing buttons to loosen the capsule. Repeat steps 8 and 9 if necessary.
  21. Hold breath:
  22. Continue to hold your breath for at least 5-10 seconds or as long as comfortably possible while removing the inhalation device from your mouth. Then breathe out.
  23. Open the inhalation device to see if any powder is left in the capsule. If there is powder left in the capsule, close the inhalation device and repeat steps 8 to 11. Most people are able to empty the capsule with one or two inhalations. Some people occasionally cough soon after inhaling the medicine. If you do, don't worry, as long as the capsule is empty, you have received the full dose.
  24. Remove capsule:
  25. After you have finished taking your daily dose of ONBREZ BREEZHALER, open the mouthpiece again, remove the empty capsule by tipping it out, and discard it. Close the inhalation device and replace the cap.
  26. Do not store the capsules in the ONBREZ BREEZHALER inhalation device.
  27. Mark daily dose tracker:
  28. On the inside of the pack there is a daily dose tracker. Put a mark in today's box if it helps to remind you of when your next dose is due.

Additional Information:

Occasionally, very small pieces of the capsule can get past the screen and enter your mouth. If this happens, you may be able to feel these pieces on your tongue. It is not harmful if these pieces are swallowed or inhaled. The chances of the capsule shattering will be increased if the capsule is pierced more than once (Step 6).

Remember:

  • Do not swallow ONBREZ BREEZHALER capsules
  • Only use the ONBREZ BREEZHALER inhalation device contained in this pack
  • ONBREZ BREEZHALER capsules must always be stored in the blister, and only removed immediately before use
  • Never place an ONBREZ BREEZHALER capsule directly into the mouthpiece of the ONBREZ BREEZHALER inhalation device
  • Do not press the piercing buttons more than once
  • Never blow into the mouthpiece of the ONBREZ BREEZHALER inhalation device
  • Always release the push buttons before inhalation
  • Never wash the ONBREZ BREEZHALER inhalation device with water. Keep it dry
  • Never take the ONBREZ BREEZHALER inhalation device apart
  • Always use the new ONBREZ BREEZHALER inhalation device that comes with your new ONBREZ BREEZHALER medication pack (use a new ONBREZ BREEZHALER inhalation device each month)
  • Do not store the capsules in the ONBREZ BREEZHALER inhalation device
  • Always keep the ONBREZ BREEZHALER inhalation device and ONBREZ BREEZHALER capsules in a dry place

Overdose:

In case of drug overdose, contact a health care practitioner, hospital emergency department or regional poison Control Centre immediately, even if there are no symptoms.

If you have accidentally inhaled too much ONBREZ BREEZHALER or if someone else accidentally inhaled your medicine, contact a doctor or hospital for advice immediately.

Show the pack of ONBREZ BREEZHALER. Medical attention may be needed.

Missed dose:

If you forget a dose, inhale the next dose on the usual time the next day. Do not take a double dose to make up for a forgotten dose.

Other related products

Desferal (Deferoxamine)

Author , posted on June 20, 2017

Category:


Desferal

Deferoxamine Mesylate

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Desferal (Deferoxamine) Dosage and Side Effects

DESFERAL is used in the treatment of following conditions, acute iron poisoning as an adjunct to the standard treatments, chronic iron overload due to frequent blood transfusion, and chronic aluminum overload in patients with end-stage kidney failure required dialysis.

Warnings and Precautions

The treatment with DESFERAL should be started and followed up by a doctor experienced in the treatment of chronic iron or aluminum overload.

BEFORE you use DESFERAL talk to your doctor or pharmacist if you:

  • have any hearing or eye sight problems. DESFERAL may cause hearing problems and eye sight problems;
  • have high blood sugar (diabetes);
  • have blood clotting problems;
  • have any neurological problems (convulsion, dementia);
  • severe kidney problem that does not required dialysis;
  • lung disease or problem breathing;
  • are pregnant or planning to become pregnant. DESFERAL can harm the unborn child, especially if it is used during the first 3 months of pregnancy. If the treatment with DESFERAL is needed, female patients who can get pregnant should use an effective birth control method before starting, while taking, and for at least one month after the last treatment with DESFERAL;
  • are breastfeeding.

DESFERAL may reduce growth rate. Patients under 16 years of age should be monitored for body weight and height every three months.

Increased risk of eye disorders have been reported in patients older than 65 years of age.

Effects on ability to drive or use machines:

DESFERAL may affect your sight or hearing, make you feel dizzy, or cause other disturbances of nervous function. If you experience such effects you should not drive or use machines.

Side Effects

Very common side effects (affecting more than 10 in 100 patients):

  • injection site reaction such as pain, swelling, reddening, itching of the skin, eschar (dead tissue that sheds from healthy skin), crust formation, small blisters, burning
  • joint or muscle pain

Common side effects (affecting more than 1 and less than 10 in 100 patients):

  • nausea
  • headache
  • itchy rash
  • fever
  • reduced growth rate, bone disorders

Uncommon side effects (affecting between 1 and 10 in 1000 patients):

  • vomiting
  • abdominal pain

Very rare side effects (affecting less than 1 in 10 000 patients):

  • diarrhea
  • skin rash
  • sensation of numbness or tingling in fingers and toes

Unknown Frequency:

  • muscle spasms
  • abnormal liver or kidney function test results
  • a low blood level of calcium, and worsening hyperparathyroidism in patients treated for aluminum overload
  • reddish-brown urine
  • low blood pressure, increased heart rate and shock

Interactions with this medication

Tell your doctor or pharmacist if you are taking or have recently taken any other medicines in addition to DESFERAL, including medicines obtained without a prescription. You may need to change the dosage or stop taking one of the medicines.

Drugs that may interact with DESFERAL include:

  • medicines containing prochlorperazine, a neuroleptic drug used to treat neurological disorders
  • vitamin C
  • erythropoietin
  • gallium-67, a medicine given before imaging (scanning, which is used in diagnosis of certain diseases)

In patients without heart failure, their doctor may tell them to take vitamin C one month before and during regular treatment with DESFERAL. The maximum daily dose of vitamin C should not exceed 200 mg for adult patients, 100 mg in older children and 50 mg for children under 10 years of age. However, their doctor also needs to monitor their heart function.

Proper Use of this medication

Your doctor has chosen the right dose and method of administration for your particular condition. Follow your doctor's instructions carefully. Make sure you use the medication exactly as your doctor tells you.

Usual dose:

Acute iron poisoning:

DESFERAL can be used in cases of poisoning with iron preparations. This treatment is carried out in hospital.

Chronic iron overload:

Daily doses of 20 to 60 mg per kilogram bodyweight. DESFERAL can be given by slow infusion under the skin (subcutaneously), by infusion into a vein (intravenously), or by injection into a muscle (intramuscularly).

Chronic aluminum overload in patients with severe kidney disease:

DESFERAL is usually given once a week by slow infusion into a vein during the last 60 minutes of a dialysis session, or 5 hours before a dialysis session, depending on the aluminum concentration in your blood.

The dose of DESFERAL is 5 mg per kilogram of bodyweight.

The duration of treatment and any change in your individual dose of DESFERAL will depend on the results of the tests carried out by your doctor.

Diagnosis of aluminum overload:

If you are receiving dialysis, your doctor will want to test whether you have aluminum overload. You will be given 5 mg of DESFERAL per kilogram of bodyweight by slow infusion into a vein during the last 60 minutes of a dialysis session. The aluminum content of blood samples taken just before this dialysis session and the next one will be determined.

Overdose:

In case of drug overdose, contact a health care practitioner, hospital emergency department or regional Poison Control Centre immediately, even if there are no symptoms.

Missed dose:

If you have missed a dose of DESFERAL, tell your doctor at once.

Other related products

Ultibro Breezhaler (Indacaterol/Glycopyrronium Bromide)

Author , posted on June 20, 2017

Category:


Ultibro Breezhaler

Glycopyrronium, Indacaterol

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Ultibro Breezhaler

Glycopyrronium, Indacaterol

Select Quantity:

Ultibro Breezhaler (Indacaterol/Glycopyrronium Bromide) Dosage and Side Effects

ULTIBRO BREEZHALER is used long term once daily to treat breathing difficulties due to a lung disease called chronic obstructive pulmonary disease (COPD).

Warnings and Precautions

Serious Warnings and Precautions

ULTIBRO BREEZHALER should only be used to treat COPD.

ULTIBRO BREEZHALER should not be used to treat asthma.

You are advised that in patients with asthma, long-acting beta2-agonist (LABA) medicines, may increase the chance of death from asthma problems. In a large asthma study, more patients who used another LABA medicine (salmeterol) died from asthma problems compared with patients who did not use that LABA medicine. This finding with salmeterol is considered a class effect of LABA, including indacaterol maleate, one of the active ingredients of ULTIBRO BREEZHALER.

BEFORE you use ULTIBRO BREEZHALER talk to your doctor, nurse or pharmacist if you:

  • Are pregnant or planning to become pregnant;
  • Are a breast-feeding mother;
  • Are an asthmatic (in this case you should not be treated with ULTIBRO BREEZHALER);
  • Have heart problems, such as rapid or irregular heart beat or abnormal electrical signal called “prolongation of the QT interval”;
  • Have high blood pressure;
  • Have seizures;
  • Have thyroid gland problems or disease;
  • Suffer from diabetes;
  • Are taking similar medicines for your lung disease;
  • Are taking any medications including eye drops, this includes medications you can buy without prescription;
  • Have problems with your kidneys;
  • Have severe liver problems;
  • Have eye problems, such as glaucoma or eye pain, blurred vision, see halos around lights or coloured images;
  • Have an enlarged prostate, problems passing urine, or painful urination;
  • Have a severe allergy to milk proteins. Ask your doctor if you are not sure;
  • Have had allergies to atropine or related medicines, for example ipratropium or tiotropium;
  • Have allergies to food or drugs.

These capsules are intended for inhalation only.

DO NOT SWALLOW.

ULTIBRO BREEZHALER should not be used more frequently than once daily. Do not exceed the prescribed dose.

This medication has been prescribed for you and should not be given to other people.

Avoid getting the drug powder into your eyes. This may result in eye pain and/or discomfort, temporary blurring of vision, and/or coloured images in association with red eyes. These may be signs of acute narrow-angle glaucoma. Should any of these symptoms develop, consult a doctor immediately.

Remember to tell any other doctor, nurse, dentist or pharmacist you consult that you are taking this medication.

Driving and Using Machines:

The occurrence of dizziness or blurred vision may influence the ability to drive and use machinery.

During the treatment with ULTIBRO BREEZHALER, tell your doctor immediately if you experience any of the following symptoms:

  • stop taking ULTIBRO BREEZHALER and tell your doctor immediately if you experience a tightness of the chest, coughing, wheezing or breathlessness immediately after inhalation of ULTIBRO BREEZHALER (signs of bronchospasm)
  • stop taking ULTIBRO BREEZHALER and tell your doctor immediately if you experience difficulties in breathing or swallowing, swelling of tongue, lips and face, hives or itching, skin rash (signs of hypersensitivity reaction). Do not use ULTIBRO BREEZHALER again before speaking with your doctor.
  • if your COPD symptoms (breathlessness, wheezing, cough) do not improve or if they worsen during your treatment.
  • stop taking ULTIBRO BREEZHALER and tell your doctor immediately if you experience eye pain or discomfort, temporary blurring of vision, visual halos or colored images in association with red eyes; these may be signs of an acute attack of narrow-angle glaucoma.

ULTIBRO BREEZHALER does not relieve sudden symptoms of COPD. Always have a short-acting bronchodilator medicine with you to treat acute symptoms. If you do not have an inhaled, short-acting bronchodilator, contact your healthcare provider to have one prescribed for you.

Get emergency medical care if:

  • breathing problems worsen quickly
  • you use your short-acting bronchodilator medicine, but it does not relieve your breathing problems

Ask your doctor, nurse or pharmacist for advice before taking any additional medicine.

Side Effects

As with all medicines, patients using ULTIBRO BREEZHALER may experience side effects, although not everybody gets them.

Side effects may include:

  • Feeling of pressure or pain in the cheeks and forehead (possible symptoms of sinusitis)
  • Runny or stuffy nose, sneezing
  • Dizziness
  • Headache
  • Cough
  • Sore throat/or mouth
  • Upset stomach, indigestion
  • Cavities
  • Pain in muscles, bones or joints
  • Pain in extremities (e.g. arms or legs)
  • Fever
  • Chest pain
  • Problem falling asleep
  • Tingling or numbness
  • Nose bleeds
  • Dry mouth
  • Skin itching/rash
  • Muscle spasm
  • Tiredness
  • Shakiness or trembling
  • Nervousness
  • Nausea, vomiting, diarrhea and abdominal pain (possible symptoms of gastroenteritis)
  • High blood pressure

If any of these affects you severely, tell your doctor, nurse or pharmacist.

ULTIBRO BREEZHALER can cause abnormal blood test results such as decreased levels of potassium and increased blood sugar. Your doctor will decide when to perform blood tests and will interpret the results.

Interactions with this medication

Tell your doctor, nurse or a pharmacist if you are taking or have recently taken any other medicines, including prescription and non-prescription drugs, eye drops, vitamins, and herbal supplements.

The following may interact with ULTIBRO BREEZHALER:

  • Medicines used in the treatment of depression or sad mood (e.g. tricyclic antidepressants, monoamine oxidase inhibitors);

  • Medicines for your lung disease which contain active substances similar (same class) to those in ULTIBRO BREEZHALER (use of these may increase the risk of experiencing possible side effects);

  • Medicines that decrease the level of potassium in your blood. These include diuretics (also known as “water tablets” and used to treat high blood pressure, e.g. hydrochlorothiazide), other bronchodilators such as methylxanthines used for breathing problems (e.g. theophylline) or steroids (e.g. prednisolone).

  • Beta-blockers used in the treatment of high blood pressure or other heart problems (e.g. propranolol) or in the treatment of glaucoma (e.g. timolol);

  • Ketoconazole (used to treat fungal infections);

  • Ritonavir (Anti-HIV medicine);

  • Erythromycin (used to treat bacterial infections);

  • Verapamil (used to treat high blood pressure, severe chest pain, irregular heartbeat).

Proper Use of this medication

Always use this medicine exactly as your doctor, nurse or pharmacist has told you. Check with your doctor, nurse or pharmacist if you are not sure.

You can inhale ULTIBRO BREEZHALER before or after food or drink.

Usual adult dose:

Inhale the contents of one capsule through the mouth each day, every day at the same time. Inhaling ULTIBRO BREEZHALER at the same time each day will help to minimize your symptoms throughout the day and night and will also help you to remember to use it.

You only need to inhale once a day to help you breathe easier because the effects of ULTIBRO BREEZHALER last for 24 hours.

Use ULTIBRO BREEZHALER even when you have no breathing problems or other symptoms of COPD.

How long to continue to take ULTIBRO BREEZHALER:

Keep using ULTIBRO BREEZHALER for as long as your doctor tells you.

COPD is a long-term disease and you should use ULTIBRO BREEZHALER every day and not only when you have breathing problems or other symptoms of COPD.

If you have questions about how long to continue your treatment with ULTIBRO BREEZHALER, talk to your doctor or your pharmacist.

Each ULTIBRO BREEZHALER pack contains:

REMEMBER:

  • Do not swallow ULTIBRO BREEZHALER capsules.
  • Only use the ULTIBRO BREEZHALER inhaler contained in this pack.
  • ULTIBRO BREEZHALER capsules must always be stored in the blister, and only removed immediately before use.
  • Never place a ULTIBRO BREEZHALER capsule directly into the mouthpiece of the ULTIBRO BREEZHALER inhaler.
  • Do not press the piercing buttons more than once.
  • Never blow into the mouthpiece of the ULTIBRO BREEZHALER inhaler.
  • Always release the push buttons before inhalation.
  • Never wash the ULTIBRO BREEZHALER inhaler with water. Keep it dry. See below “How to clean your inhaler:”.
  • Never take the ULTIBRO BREEZHALER inhaler apart.
  • Always keep the ULTIBRO BREEZHALER inhaler and ULTIBRO BREEZHALER capsules in a dry place.
  • Avoid getting the drug powder in your eyes.

How to clean your inhaler:

Never wash your inhaler with water. If you want to clean your inhaler wipe the mouthpiece inside and outside with a clean, dry, lint-free cloth to remove any powder residue. Keep the inhaler dry.

Overdose:

If you think you have inhaled too much ULTIBRO BREEZHALER, contact your doctor, nurse, pharmacist, hospital emergency department or regional Poison Control Centre immediately, even if there are no symptoms.

If you accidentally take a larger dose of ULTIBRO BREEZHALER you may feel shaky, have a headache, or feel like your heart is beating faster than usual. Talk to your doctor or pharmacist right away if this occurs.

Missed dose:

If you forget to inhale a dose, inhale a dose as soon as possible on the same day. However, do not inhale two doses on the same day. Then inhale the next dose as usual.

Other related products

Dermotic Oil Ear Drops (Fluocinolone)

Author , posted on June 20, 2017

Category:


Dermotic Oil Ear Drops

Fluocinolone Acetonide

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Dermotic (Fluocinolone) Dosage and Side Effects

DERMOTIC is used to treat eczema of the outer ear (also known as chronic itchy ear).

Warnings and Precautions

Before using DERMOTIC EAR DROPS, tell your doctor or pharmacist if you are allergic to it; or to other corticosteroids (e.g., hydrocortisone, prednisone); or if you have any other allergies. This product may contain inactive ingredients (such as peanut oil), which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history.

Do not use if there is an infection or sore in the area to be treated. Skin infections can become worse when this medication is used. Tell your doctor promptly if redness, swelling, or irritation does not improve.

During pregnancy, this product should be used only when clearly needed. Discuss the risks and benefits with your doctor.

It is not known whether this drug passes into breast milk when applied to the skin. Similar medications pass into breast milk when taken by mouth. Consult your doctor before breast-feeding.

Side Effects

Stinging, burning, irritation, dryness, or redness at the application site may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Interactions with this medication

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor or pharmacist first.

Before using this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use.

Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Proper Use of this medication

To apply ear drops, wash your hands first. To avoid contamination, do not touch the dropper tip or let it touch your ear or any other surface. Lie on your side or tilt the affected ear upward. Hold the dropper directly over the ear, and place the prescribed number of drops into the ear canal, usually twice a day or as directed by your doctor. To help the drops roll into the ear of an adult, hold the earlobe up and back. In children, hold the earlobe down and back. Keep the head tilted for about 1 minute, or insert a soft cotton plug if so directed. Remove the plug after 1 minute. Repeat for the other ear if so directed. Do not rinse the dropper. Replace the cap after use. Do not bandage, cover, or wrap the area unless directed to do so by your doctor.

Avoid getting this medication in the eyes, nose, or mouth. If you get the medication in these areas, rinse with plenty of water.

Dosage is based on your medical condition and response to treatment.

Use this medication regularly to get the most benefit from it. To help you remember, use it at the same times each day.

Use this medication only for the condition for which it was prescribed. Do not use it for longer than prescribed.

Tell your doctor if your condition persists or worsens after 2 weeks.

Other related products

Dermatop (Prednicarbate)

Author , posted on June 20, 2017

Category:


Dermatop Emollient Cream

Prednicarbate

Select Quantity:

Dermatop (Prednicarbate) Dosage and Side Effects

DERMATOP topical is used to treat the inflammation and itching caused by a number of skin conditions such as allergic reactions, eczema, and psoriasis.

Warnings and Precautions

Do not cover treated skin areas with a bandage or other covering unless your doctor has told you to. If you are treating the diaper area of a baby, do not use plastic pants or tight-fitting diapers. Covering the skin that is treated with DERMATOP topical can increase the amount of medicine your skin absorbs, which may lead to unwanted side effects. Follow your doctor's instructions.

Do not use this medication on a child without a doctor's advice. Children are more likely to absorb large amounts of a topical steroid through the skin. Steroid absorption in children may cause unwanted side effects, or a delay in growth with long-term use. Talk with your doctor if you think your child is not growing at a normal rate while using this medication over a long treatment period.

Contact your doctor if your condition does not improve within 2 weeks of using this medicine, or if you develop signs of a bacterial, fungal, or viral skin infection.

You should not use this medication if you are allergic to DERMATOP .

To make sure you can safely use DERMATOP topical, tell your doctor if you have any type of skin infection.

Also tell your doctor if you have diabetes. Topical steroid medicines absorbed through the skin may increase the glucose (sugar) levels in your blood or urine.

FDA pregnancy category C. It is not known whether DERMATOP topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.

DERMATOP  topical cream or ointment contains an ingredient that can break down latex rubber, such as a condom or diaphragm. This can damage these items and make them less effective in preventing pregnancy or sexually transmitted disease. Avoid getting DERMATOP topical on a condom or diaphragm. This medication should not be used in the vagina or rectum.

It is not known whether DERMATOP topical passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Side Effects

Stop using DERMATOP topical and call your doctor at once if you have a serious side effect such as:

  • blurred vision, or seeing halos around lights;
  • mood changes;
  • sleep problems (insomnia);
  • weight gain, puffiness in your face; or
  • muscle weakness, feeling tired.

Less serious side effects may include:

  • mild skin rash, itching, burning, swelling, or dryness;
  • thinning or softening of your skin;
  • skin rash or irritation around your mouth;
  • swollen hair follicles;
  • numbness or tingling;
  • changes in color of treated skin;
  • blisters, pimples, or crusting of treated skin; or
  • stretch marks.

Interactions with this medication

DERMATOP topical should not be used to treat any skin condition your doctor has not prescribed it for.  Avoid using DERMATOP topical to treat skin on your face, underarms, or groin area without your doctor's advice.

Avoid getting this medication in your eyes, nose, mouth, rectum, or vagina. If this does happen, rinse with water. Do not use DERMATOP topical on broken or infected skin. Also avoid using this medication in open wounds.

It is not likely that other drugs you take orally or inject will have an effect on topically applied DERMATOP. But many drugs can interact with each other. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

Proper Use of this medication

Apply a small amount to the affected area and rub it gently into the skin. Do not use this medication over a large area of skin. Do not cover treated skin areas with a bandage or other covering unless your doctor has told you to. If you are treating the diaper area of a baby, do not use plastic pants or tight-fitting diapers. Covering the skin that is treated with DERMATOP topical can increase the amount of medicine your skin absorbs, which may lead to unwanted side effects. Follow your doctor's instructions.

Contact your doctor if your condition does not improve within 2 weeks of using this medicine, or if you develop signs of a bacterial, fungal, or viral skin infection. It is important to use DERMATOP topical regularly to get the most benefit.

An overdose of DERMATOP topical is not expected to produce life-threatening symptoms. However, long-term use of high steroid doses can lead to symptoms such as thinning skin, easy bruising, changes in the shape or location of body fat (especially in your face, neck, back, and waist), increased acne or facial hair, menstrual problems, impotence, or loss of interest in sex.

Use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.

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