Duac (Benzoyl Peroxide / Clindamycin)

Author , posted on July 2, 2017

Category:


Clindoxyl Gel

Benzoyl Peroxide, Clindamycin Phosphate

Select Quantity:

Clindoxyl Gel

Benzoyl Peroxide, Clindamycin Phosphate

Select Quantity:

Benzoyl Peroxide/Clindamycin Phosphate Gel (Generic)

Benzoyl Peroxide, Clindamycin Phosphate

Select Quantity:

 Duac (Benzoyl Peroxide/Clindamycin) Dosage and Side Effects

DUAC is used to treat acne.

Warnings and Precautions

This medicine can cause a rare but serious allergic reaction or severe skin irritation. Stop using this medicine and get emergency medical help if you have: hives, itching; difficulty breathing, feeling light-headed; or swelling of your face, lips, tongue, or throat.

You should not use this medicine if you are allergic to DUAC.

Although this medicine is applied to the skin, your body may absorb enough clindamycin to cause serious side effects. You may not be able to use this medicine if you have:

  • inflammation of your intestines (also called enteritis);
  • ulcerative colitis; or
  • if you have ever had severe diarrhea caused by antibiotic medicine.

It is not known whether DUAC topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medicine.

It is not known whether DUAC topical passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Side Effects

Benzoyl peroxide can cause a rare but serious allergic reaction or severe skin irritation. These reactions may occur just a few minutes after you apply the medicine, or within a day or longer afterward.

Stop using this medicine and get emergency medical help if you have signs of an allergic reaction: hives, itching; difficulty breathing, feeling light-headed; swelling of your face, lips, tongue, or throat.

Stop using this medicine and call your doctor at once if you have:

  • severe redness, burning, stinging, or peeling of treated skin areas; or
  • diarrhea that is watery or bloody.

Common side effects may include:

  • mild burning or stinging;
  • itching or tingly feeling;
  • dryness or peeling of treated skin; or
  • redness or other irritation.

Interactions with this medication

Avoid using skin products that can cause irritation, such as harsh soaps, shampoos, or skin cleansers, hair coloring or permanent chemicals, hair removers or waxes, or skin products with alcohol, spices, astringents, or lime.

Avoid using other medications on the areas you treat with DUAC topical unless your doctor tells you to.

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop using DUAC topical and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Avoid exposure to sunlight or tanning beds. This medication can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

Avoid using sunscreen containing PABA on the same skin treated with DUAC topical, or skin discoloration may occur.

Benzoyl peroxide can bleach hair or fabrics. Do not let this medicine come into contact with clothing, hair, or colored towels or bed linens.

It is not likely that other drugs you take orally or inject will have an effect on topically applied DUAC. But many drugs can interact with each other. Tell each of your health care providers about all medicines you use, including prescription and over-the-counter medicines, vitamins, and herbal products.

Proper Use of this medication

Follow all directions on your prescription label. Do not use this medicine in larger or smaller amounts or for longer than recommended.

Using more medicine or applying it more often than prescribed will not make it work any faster, and may increase side effects.

Benzoyl peroxide can cause a rare but serious allergic reaction or severe skin irritation. Before you start using this medicine, you may choose to apply a "test dose" to see if you have a reaction. Apply a very small amount of the medicine to 1 or 2 small acne areas every day for 3 days in a row. If there is no reaction, begin using the full prescribed amount on the 4th day.

Wash your hands before and after applying this medicine.

Wash your face with a mild cleanser (not soap) and pat the skin dry with a clean towel.

DUAC topical is usually applied twice daily, in the morning and evening.

Avoid getting this medicine in your eyes, mouth, or nose (or in the creases of your nose), or on your lips. If it does get into any of these areas, wash with water. Do not apply this medicine to sunburned, windburned, dry, chapped, irritated, or broken skin.

It may take several weeks before your symptoms improve. Keep using the medication as directed and tell your doctor if your symptoms do not improve.

If you receive more than one supply of Acanya or Duac gel, store the unopened container in a refrigerator until you are ready to start using it. Do not freeze.

Once in use, store the gel at room temperature away from moisture and heat. Do not freeze. Throw away any unused medicine after the expiration date on the label has passed. Duac has an expiration date of 60 days. Acanya has an expiration date of 10 weeks. BenzaClin has an expiration date of 3 months.

Seek emergency medical attention or call the Poison Help line.

Overdose symptoms include bloody or watery diarrhea, which may result if you absorb this medicine through your skin by applying too much.

Apply 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.

Other related products

Diclegis (Pyridoxine/Doxylamine)

Author , posted on July 2, 2017

Category:


Diclegis (Pyridoxine/Doxylamine) Dosage and Side Effects

DICLEGIS is used to treat nausea and vomiting during pregnancy, sometimes called morning sickness.

Proper Use of this medication

Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Do not crush, chew, or break a delayed-release tablet. Swallow it whole.

DICLEGIS is usually taken at bedtime on an empty stomach, at least 2 hours after a meal.

If your symptoms do not improve, you may need to take 1 tablet in the morning, 1 tablet in the afternoon, and 2 tablets at bedtime. Follow your doctor's instructions.

Call your doctor if your symptoms get worse while using DICLEGIS. Severe or ongoing vomiting can cause you to become dehydrated which can lead to serious medical problems.

Overdose symptoms may include dry mouth, extreme drowsiness or dizziness, confusion, restless feeling, dilated pupils, rapid heartbeats, seizure (convulsions), or unexplained muscle pain or weakness with fever and dark colored urine.

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

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.

Common side effects may include:

  • drowsiness.

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

Warnings and Precautions

Do not use DICLEGIS if you have used an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

Do not use DICLEGIS if you have used an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

You should not use this medicine if you are allergic to doxylamine or pyridoxine, or to other antihistamines such as Benadryl or Dramamine.

To make sure this medicine is safe for you, tell your doctor if you have:

  • asthma or other breathing disorder;
  • glaucoma, increased pressure inside your eye;
  • blockage in your digestive tract (stomach or intestines);
  • a stomach ulcer; or
  • bladder obstruction or other urination problems.

FDA pregnancy category A. DICLEGIS is not expected to harm an unborn baby.

DICLEGIS can pass into breast milk and may harm a nursing baby. You should not breast-feed while using this medicine.

Do not give this medication to anyone under 18 years old without medical advice.

Interactions with this medication

DICLEGIS may impair your thinking or reactions. Avoid driving or operating machinery until you know how this medicine will affect you.

Avoid drinking alcohol. It can increase drowsiness caused by DICLEGIS.

Many medicines available over the counter can increase drowsiness caused by DICLEGIS. Ask a doctor or pharmacist before using any cough/cold, allergy, pain, or sleep medication. Severe drowsiness can cause falls or other accidents.

Do not take any medicine without your doctor's advice while you are pregnant.

Taking this medicine with other drugs that make you sleepy can worsen this effect. Ask your doctor before taking DICLEGIS with any medications you use to treat depression, mental illness, or seizures.

Other drugs may interact with DICLEGIS, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

Other related products

Didronel (Etidronate)

Author , posted on July 2, 2017

Category:


PRODUCT NOT AVAILABLE

Didronel

Etidronate Disodium

Select Quantity:

Didronel (Etidronate) Dosage and Side Effects

DIDRONEL is in a group of medicines called bisphosphonates (bis FOS fo nayts). It alters the cycle of bone formation and breakdown in the body.

DIDRONEL is used to treat Paget's disease, and to treat conditions of irregular bone growth due to hip fracture or spinal cord injury.

Proper Use of this medication

Do not crush, chew, or suck the pill. Swallow it whole.

Take each DIDRONEL tablet with a full glass (6 to 8 ounces) of water. Use only plain water (not mineral water) when taking an DIDRONEL tablet.

For at least the first 2 hours after taking DIDRONEL, do not eat or drink anything other than plain water, and do not take any other medicines including vitamins or mineral supplements.

It is important to take DIDRONEL regularly to get the most benefit.

If you need to have any dental work (especially surgery), tell the dentist ahead of time that you are using DIDRONEL. You may need to stop using the medicine for a short time.

After you stop taking DIDRONEL, you must stay off the medication for at least 90 days before starting DIDRONEL therapy again.

Your doctor will need to check your progress while you are using DIDRONEL.

DIDRONEL is only part of a complete program of treatment that may also include taking calcium and vitamin supplements. Follow your diet, medication, and exercise routines very closely.

Store at room temperature away from moisture and heat.

Seek emergency medical attention or call the Poison Help line.

Overdose symptoms may include vomiting, numbness or tingly feeling around your mouth, fast or slow heart rate, muscle tightness or contraction, overactive reflexes.

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

Side Effects

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

Stop using DIDRONEL and call your doctor at once if you have:

  • painful or difficult swallowing;
  • severe heartburn, burning pain in your upper stomach, or coughing up blood;
  • severe joint, bone, or muscle pain;
  • jaw pain, numbness, or swelling;
  • severe diarrhea; or
  • severe skin reaction--fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Common side effects may include:

  • mild diarrhea;
  • headache, confusion;
  • muscle cramps, joint pain; or
  • numbness or tingly feeling.

Warnings and Precautions

You should not take this medicine if you have a condition called osteomalacia (softening of the bones), or a problem with the movement of muscles in your esophagus.

To make sure DIDRONEL is safe for you, tell your doctor if you have:

  • diarrhea;
  • a bone fracture;
  • trouble swallowing;
  • a stomach or esophageal ulcer or disease; or
  • kidney disease.

In rare cases, this medicine may cause bone loss (osteonecrosis) in the jaw. Symptoms include jaw pain or numbness, red or swollen gums, loose teeth, or slow healing after dental work. The longer you use DIDRONEL, the more likely you are to develop this condition.

Osteonecrosis of the jaw may be more likely if you have cancer or received chemotherapy, radiation, or steroids. Other risk factors include blood clotting disorders, anemia (low red blood cells), and a pre existing dental problem.

Talk with your doctor about the risks and benefits of using this medication.

It is not known whether DIDRONEL will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.

It is not known whether DIDRONEL passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Interactions with this medication

Avoid drinking milk or eating dairy products within 2 hours after taking DIDRONEL. Also avoid taking supplements that contain calcium, magnesium, iron, or aluminum (such as in multivitamins with iron, and in many types of antacids).

Tell your doctor about all your current medicines and any you start or stop using, especially:

  • a blood thinner--warfarin, Coumadin, Jantoven.

This list is not complete. Other drugs may interact with DIDRONEL, including prescription and over-the-counter medicines, vitamins, and herbal products.

Other related products

Depakene (Valproic Acid)

Author , posted on July 2, 2017

Category:


Depakene

Valproic Acid

Select Quantity:

Valproic Acid (Generic)

Valproic Acid

Select Quantity:
Select Quantity:

Valproic Syrup (Generic)

Valproic Acid

Select Quantity:

Depakene (Valproic Acid) Dosage and Side Effects

DEPAKENE is used to control epilepsy.

Proper Use of this medication

Please consult your doctor before taking any other medication, including over-the-counter medicines. Some drugs can produce various side effects when they are used in combination with DEPAKENE.

It is important to keep your appointments for medical checkups.

The doctor may need to take blood tests to measure the amount of DEPAKENE in your blood when adjusting your medications.

Usual dose:

It is very important to take DEPAKENE exactly as instructed by your doctor.

The recommended starting dose of DEPAKENE will be decided by your doctor based on your weight, your seizures or manic episodes and your concomitant medications. Be sure to tell your doctor all the prescription and over the counter medications that you are currently taking. Your doctor will gradually increase the dosage until your condition is well controlled without experiencing side effects. You should carefully follow the instructions that were given to you and not change your dose without consulting with your doctor.

DEPAKENE may be taken with or without food.

Overdose:

If you accidentally take an overdose of DEPAKENE, you should contact your doctor or nearest hospital emergency, or your Regional Poison Control Centre, even though you may not feel sick.

Missed dose:

Do not suddenly stop taking your medicine because of the risk of increasing your epileptic seizures.

If you miss a dose, you should not try to make up for it by doubling up on your next dose. You should take your next regularly scheduled dose and try not to miss any more doses.

Side Effects

You should check with your doctor or pharmacist right away if you notice any bothersome or unusual effects while taking DEPAKENE.

The most commonly reported adverse reactions include nausea, vomiting, indigestion, sleepiness, headache, diarrhea, weakness, tremor and dizziness. Changes in hair are also reported, such as hair loss or in increase in hair on face, chest and back. If any of these affect you severely, contact your doctor or pharmacist.

You should know that this does not mean that you will experience such effects, because people can react in different ways to the same medicine.

Warnings and Precautions

Serious Warnings and Precautions

  • Hepatotoxicity: liver failure resulting in death has occurred in patients receiving DEPAKENE. These incidents usually occurred during the first 6 months of treatment with DEPAKENE. Patients taking several anticonvulsant drugs, children, those with a history of liver disease, metabolic disorders, severe seizure disorders accompanied by mental retardation, and those with brain disease may be at particular risk. Experience has indicated that children under the age of 2 years are at a considerably increased risk of developing fatal hepatotoxicity, especially those on multiple anticonvulsants.

  • Teratogenicity: DEPAKENE can produce birth defects to an unborn baby. Accordingly, the use of DEPAKENE in women of childbearing potential requires that the benefits of its use be weighed against the risk of injury to the fetus.

  • Pancreatitis: cases of life threatening pancreas disorder have been reported in both children and adults receiving DEPAKENE. Some cases have occurred shortly after first use as well as after several years of use. Abdominal pain, nausea, vomiting and/or anorexia can be symptoms of pancreatitis that require immediate medical evaluation.

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

  • you have a history of, or suffer from a liver disease, such as jaundice (yellowing of the skin and eyes);

  • you have ever had an unusual or allergic reaction to DEPAKENE (including fever or rash);

  • you are allergic to any component of DEPAKENE capsules or oral solution;

  • you are pregnant or are planning to become pregnant;

  • you are breast-feeding (nursing); DEPAKENE passes into breast milk;

  • you are taking any other prescription or over the counter medicine;

  • you have kidney disease;

  • you have other medical conditions including a history of unexplained coma, intellectual disability or any type of brain dysfunction;

  • you have a psychiatric disorder or have thoughts of suicide;

  • you consume alcohol on a regular basis.

Precautions while taking DEPAKENE:

  • Your doctor will monitor your response to DEPAKENE on a regular basis. However, if your seizures get worse, you should tell your doctor immediately.

  • Since DEPAKENE may cause poor coordination and/or drowsiness, you should not engage in hazardous activities, such as driving and operating machinery, until you know that you don’t become drowsy from the drug.

  • You should not stop taking your medication unless directed by your doctor. You should always check that you have an adequate supply of DEPAKENE. You should remember that this medicine was prescribed only for you; it should never be given to anyone else.

Women of Childbearing Potential:

  • All women of childbearing age who are being treated with DEPAKENE should talk to their healthcare providers about using other possible treatments instead of DEPAKENE. If the decision is made to use DEPAKENE, you must use an effective method of birth control (contraception). You should talk to your doctor about the best kind of birth control to use while you are taking DEPAKENE.

Pregnant Women:

  • If you take DEPAKENE during pregnancy, your child has a higher risk for birth defects and adverse effects on IQ and brain development, which can begin early in the pregnancy, even before you know that you are pregnant.

  • There may be other medications to treat your condition that have a lower chance of birth defects.

  • If you are planning to become pregnant, or if you become pregnant while taking DEPAKENE, you should promptly inform your doctor. Do not suddenly stop taking the drug. Appropriate treatment options will need to be discussed with your physician to ensure the benefits outweigh the risks.

Interactions with this medication

Serious Drug Interactions

  • Rare cases of coma have been reported in patients receiving DEPAKENE alone or when taken with phenobarbital.

  • Serious skin reactions (such as conditions called Stevens-Johnson syndrome and Toxic Epidermal Necrolysis) have been reported when DEPAKENE and lamotrigine were taken together.

Drugs that may interact with DEPAKENE include:

  • anticonvulsants such as carbamazepine, lamotrigine, primidone, topiramate, felbamate, phenytoin, ethosuximide, phenobarbital;

  • anticoagulants such as acetylsalicylic acid, warfarin, dicumarol;

  • benzodiazepines such as diazepam, lorazepam, clonazepam;

  • some medicines used to treat infections such as rifampin;

  • some medicines used to treat diabetes such as tolbutamide;

  • some HIV-antiviral medication such as zidovudine;

  • any of the group of antibiotics in the carbapenem class such as doripenem, ertapenem, imipenem, meropenem;

  • some medicines used to treat heartburn and peptic ulcers such as cimetidine;

  • medicines used to treat depression such as Selective Serotonin Re-Uptake Inhibitors (SSRIs), Monoamine Oxidase Inhibitors (MAOIs), Tricyclic antidepressants such as amitriptyline, nortriptyline;

  • antipsychotics.

Other related products

DDAVP Nasal Spray (Desmopressin)

Author , posted on July 2, 2017

Category:


Minirin Nasal Spray

Desmopressin Acetate

Select Quantity:

Desmopressin Nasal Spray (Generic)

Desmopressin Acetate

Select Quantity:

Desmopressin Nasal Spray (Generic)

Desmopressin Acetate

Select Quantity:

DDAVP (Desmopressin) Dosage and Side Effects

DDAVP Tablets reduce the amount of urine so a child's bladder will not fill up; therefore, a child will not wet the bed at night.

Proper Use of this medication

How many DDAVP Tablets should be used?

Take the medication at the dose prescribed by your physician 1 hour before bedtime. Use the following dosage plan or one that has been recommended by your physician.

Step 1: For the first 3 nights:

Take 1 tablet (1×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 1 tablet each night, continue this way. Do NOT increase the dose.

If the child is NOT dry for these 3 nights, move to Step 2.

Step 2: Nights 4, 5 and 6:

Take 2 tablets (2×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 2 tablets each night, continue this way. Do NOT increase the dose.

If the child is NOT dry for these 3 nights, move to Step 3.

Step 3: Nights 7, 8 and 9:

Take 3 tablets (3×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 3 tablets each night, continue this way. Do NOT increase the dose.

If your child is not dry every night after taking 3 tablets each night for 3 nights, see the “What should I do if ...?” section below or visit your doctor to find out why the medicine has not worked.

What should I do if ...?

The child is still wetting the bed:

  • Make sure the child is taking the correct number of tablets each night.

  • Limit the number of drinks the child has after supper.

  • If it's still not working, call your doctor.

Side Effects

As with all medicines, side effects may be experienced. With DDAVP Tablets, these may include headache, dizziness, rash, and mild abdominal cramps. These have occurred usually when the medication is being adjusted. Once you are taking the right amount of medicine for your condition, these side effects will usually go away. Tell your doctor about any side effects you experience.

Warnings and Precautions

Infrequently, high doses of DDAVP have produced transient headache and nausea. Nasal congestion, rhinitis, flushing and mild abdominal cramps have been reported. These symptoms disappeared with reduction in dosage. Please contact your physician should your child experience any side effects. For DDAVP to work at its best, it is very important to limit the number of drinks the child has after supper, especially 1 hour before bedtime. As most children sleep between 8 to 12 hours, further fluid restriction is not required. In the event the child wakes up during the night, liquid intake should be restricted.

Interactions with this medication

Tell your child's doctor or pharmacist in the unlikely event your child is taking any of the following medications (they are adult medications known to cause water retention and should be avoided when taking DDAVP); clofibrate, chlorpromazine, carbamazapine, tricyclic antidepressants (such as amitriptyline, nortriptyline), selective serotonin reuptake inhibitors (SSRIs for example, fluoxetine or Prozac, paroxetine or Paxil, sertraline or Zoloft, fluvoxamine or Luvox, citalopram or Celexa), nonsteroidal anti-inflammatory drugs (NSAIDs such as etodolac or Ultradol, ibuprofen or Advil or Motrin, naprosen or Naprosyn), celecoxib or Celebrex) and loperamide or Imodium.

Other related products

DDAVP Melt (Desmopressin)

Author , posted on July 2, 2017

Category:


DDAVP Melt

Desmopressin

Select Quantity:
Select Quantity:
Select Quantity:

DDAVP (Desmopressin) Dosage and Side Effects

DDAVP Tablets reduce the amount of urine so a child's bladder will not fill up; therefore, a child will not wet the bed at night.

Proper Use of this medication

How many DDAVP Tablets should be used?

Take the medication at the dose prescribed by your physician 1 hour before bedtime. Use the following dosage plan or one that has been recommended by your physician.

Step 1: For the first 3 nights:

Take 1 tablet (1×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 1 tablet each night, continue this way. Do NOT increase the dose.

If the child is NOT dry for these 3 nights, move to Step 2.

Step 2: Nights 4, 5 and 6:

Take 2 tablets (2×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 2 tablets each night, continue this way. Do NOT increase the dose.

If the child is NOT dry for these 3 nights, move to Step 3.

Step 3: Nights 7, 8 and 9:

Take 3 tablets (3×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 3 tablets each night, continue this way. Do NOT increase the dose.

If your child is not dry every night after taking 3 tablets each night for 3 nights, see the “What should I do if ...?” section below or visit your doctor to find out why the medicine has not worked.

What should I do if ...?

The child is still wetting the bed:

  • Make sure the child is taking the correct number of tablets each night.

  • Limit the number of drinks the child has after supper.

  • If it's still not working, call your doctor.

Side Effects

What are the possible side effects of DDAVP Tablets?

As with all medicines, side effects may be experienced. With DDAVP Tablets, these may include headache, dizziness, rash, and mild abdominal cramps. These have occurred usually when the medication is being adjusted. Once you are taking the right amount of medicine for your condition, these side effects will usually go away. Tell your doctor about any side effects you experience.

Warnings and Precautions

Infrequently, high doses of DDAVP have produced transient headache and nausea. Nasal congestion, rhinitis, flushing and mild abdominal cramps have been reported. These symptoms disappeared with reduction in dosage. Please contact your physician should your child experience any side effects. For DDAVP to work at its best, it is very important to limit the number of drinks the child has after supper, especially 1 hour before bedtime. As most children sleep between 8 to 12 hours, further fluid restriction is not required. In the event the child wakes up during the night, liquid intake should be restricted.

Interactions with this medication

Tell your child's doctor or pharmacist in the unlikely event your child is taking any of the following medications (they are adult medications known to cause water retention and should be avoided when taking DDAVP); clofibrate, chlorpromazine, carbamazapine, tricyclic antidepressants (such as amitriptyline, nortriptyline), selective serotonin reuptake inhibitors (SSRIs for example, fluoxetine or Prozac, paroxetine or Paxil, sertraline or Zoloft, fluvoxamine or Luvox, citalopram or Celexa), nonsteroidal anti-inflammatory drugs (NSAIDs such as etodolac or Ultradol, ibuprofen or Advil or Motrin, naprosen or Naprosyn), celecoxib or Celebrex) and loperamide or Imodium.

Other related products

DDAVP (Desmopressin)

Author , posted on July 2, 2017

Category:


DDAVP

Desmopressin Acetate

Select Quantity:

DDAVP

Desmopressin Acetate

Select Quantity:

DDAVP

Desmopressin Acetate

Select Quantity:
Select Quantity:

DDAVP

Desmopressin Acetate

Select Quantity:

Desmopressin (Generic)

Desmopressin

Select Quantity:
Select Quantity:

Desmopressin (Generic)

Desmopressin Acetate

Select Quantity:
Select Quantity:

DDAVP (Desmopressin) Dosage and Side Effects

DDAVP Tablets reduce the amount of urine so a child's bladder will not fill up; therefore, a child will not wet the bed at night.

Proper Use of this medication

How many DDAVP Tablets should be used?

Take the medication at the dose prescribed by your physician 1 hour before bedtime. Use the following dosage plan or one that has been recommended by your physician.

Step 1: For the first 3 nights:

Take 1 tablet (1×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 1 tablet each night, continue this way. Do NOT increase the dose.

If the child is NOT dry for these 3 nights, move to Step 2.

Step 2: Nights 4, 5 and 6:

Take 2 tablets (2×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 2 tablets each night, continue this way. Do NOT increase the dose.

If the child is NOT dry for these 3 nights, move to Step 3.

Step 3: Nights 7, 8 and 9:

Take 3 tablets (3×0.2 mg) 1 hour before bedtime.

If the child is dry for 3 nights taking 3 tablets each night, continue this way. Do NOT increase the dose.

If your child is not dry every night after taking 3 tablets each night for 3 nights, see the “What should I do if ...?” section below or visit your doctor to find out why the medicine has not worked.

What should I do if ...?

The child is still wetting the bed:

  • Make sure the child is taking the correct number of tablets each night.

  • Limit the number of drinks the child has after supper.

  • If it's still not working, call your doctor.

Side Effects

As with all medicines, side effects may be experienced. With DDAVP Tablets, these may include headache, dizziness, rash, and mild abdominal cramps. These have occurred usually when the medication is being adjusted. Once you are taking the right amount of medicine for your condition, these side effects will usually go away. Tell your doctor about any side effects you experience.

Warnings and Precautions

Infrequently, high doses of DDAVP have produced transient headache and nausea. Nasal congestion, rhinitis, flushing and mild abdominal cramps have been reported. These symptoms disappeared with reduction in dosage. Please contact your physician should your child experience any side effects. For DDAVP to work at its best, it is very important to limit the number of drinks the child has after supper, especially 1 hour before bedtime. As most children sleep between 8 to 12 hours, further fluid restriction is not required. In the event the child wakes up during the night, liquid intake should be restricted.

Interactions with this medication

Tell your child's doctor or pharmacist in the unlikely event your child is taking any of the following medications (they are adult medications known to cause water retention and should be avoided when taking DDAVP); clofibrate, chlorpromazine, carbamazapine, tricyclic antidepressants (such as amitriptyline, nortriptyline), selective serotonin reuptake inhibitors (SSRIs for example, fluoxetine or Prozac, paroxetine or Paxil, sertraline or Zoloft, fluvoxamine or Luvox, citalopram or Celexa), nonsteroidal anti-inflammatory drugs (NSAIDs such as etodolac or Ultradol, ibuprofen or Advil or Motrin, naprosen or Naprosyn), celecoxib or Celebrex) and loperamide or Imodium.

Other related products

Cytomel (Liothyronine)

Author , posted on July 2, 2017

Category:


Cytomel

Liothyronine Sodium

Select Quantity:
Select Quantity:

Cytomel

Liothyronine Sodium

Select Quantity:

Liothyronine (Generic)

Liothyronine Sodium

Select Quantity:
Select Quantity:

Cytomel (Liothyronine) Dosage and Side Effects

CYTOMEL is used for the treatment of mild to severe hypothyroidism and enlarged thyroid gland.

Proper Use of this medication

You should take CYTOMEL as prescribed by your doctor. Treatment is usually started with a low dose of CYTOMEL, then increased gradually according to your response.

Overdose:

In case of drug overdose, contact your doctor or a Poison Control Centre, or go to the emergency room of the hospital near you immediately, even if there are no symptoms.

Missed dose:

If you miss a dose, take it as soon as you remember on the same day. Skip that dose if you do not remember until the next day.

Side Effects

Side effects with CYTOMEL may include symptoms of hyperthyroidism as follows: Headache, excessive sweating, fatigue, increased appetite, weight loss, fever, nervousness, anxiety, irritability, insomnia, cardiac arrhythmias (heartbeats which are irregular or too fast), angina pectoris (chest pain), diarrhea and menstrual irregularities.

Tell your doctor about any other side effect that is not included above or if you have any question. Your doctor may ask you stop taking CYTOMEL until the symptoms disappear, and re-start after one or two days at a lower dose.

 

Warnings and Precautions

Serious Warnings and Precautions

CYTOMEL, like other thyroid hormones, should not be used for the treatment of obesity or for weight loss, either alone or with other medicines. At normal doses, CYTOMEL does not reduce body weight and at higher doses, it can produce serious or even life-threatening side effects.

Before or While you use CYTOMEL talk to your doctor if you have the following conditions:

any heart problems, such as a heart attack, angina pectoris (chest pain)

  • a history problem with thyroid (myxedema), or adrenal or pituitary gland
  • kidney disease
  • high blood sugar (diabetes)
  • decreased development of sexual organs (hypogonadism)
  • bone thinning (osteoporosis)
  • pregnant or planning to become pregnant
  • breast feeding
  • blood clotting problem

Interactions with this medication

Before or while you use CYTOMEL tell your doctor or pharmacist about all other medications you take including medications that you bought without a prescription, vitamins, and natural products. Particularly if you are taking the following:

  • Blood thinner (anticoagulants)

  • Medications for high cholesterol levels such as lovastatin, cholestyramine, clofibarate

  • Medications for high blood sugar or insulin

  • Medications that contain estrogen such as birth control pills

  • Amiodarone

  • Medicines that contain iodine such as radiographic contrast agents

  • Heroin/methadone

  • 5-fluorouracil, mitotane, tamoxifen

  • Tricyclic antidepressant such as imipramine

  • Digoxin (digitalis)

  • Cyokines such as interferon-alpha, interleukin-2

  • Growth hormones

  • Ketamine

  • Theophylline

  • Diazepam

  • Ethionamide

  • Metoclopramide

  • Perphanazine

  • Resorcinol (topical products)

  • Para-aminosalicylate sodium

Some medicines may interfere with blood tests done to determine thyroid hormone levels (thyroid function tests). It is important to inform your doctor of all medicines you are taking before and at the time of blood tests.

The following drugs are known to interfere with laboratory tests performed in patients on thyroid hormone therapy:

  • Androgens (male hormones)

  • Corticosteroids (eg., prednisone, dexamethasone)

  • Estrogens and estrogen-containing oral contraceptives (birth control pills)

  • Preparations containing iodine

  • Salicylates (eg., aspirin)

Other related products

Cyklokapron (Tranexamic Acid)

Author , posted on July 2, 2017

Category:


Cyklokapron

Tranexamic Acid

Select Quantity:

Tranexamic Acid (Generic)

Tranexamic Acid

Select Quantity:

Tranexamic Acid (Generic)

Tranexamic Acid

Select Quantity:

Cyklokapron (Tranexamic Acid) Dosage and Side Effects

CYKLOKAPRON is used to stop excessive bleeding after an operation or to assist with blood clotting.

Proper Use of this medication

Usual dose:

Take CYKLOKAPRON exactly as directed by your health care professional. Always take the number of tablets your doctor tells you.

The usual adult dose is 2-3 tablets two-three times daily.

Depending on why you have been given these tablets, your dose may be different.

The dose for children is calculated according to body weight (25 mg/kg).

Patients with kidney disease should receive lower doses.

CYKLOKAPRON solution for injection will usually be given to you by slow injection into a vein as a bolus intravenous (IV) dose over 5 minutes or as an IV drip. Your doctor will decide the best dose for you, based on your weight.

It should be inspected visually for clarity, particulate matter, precipitation, discolouration, and leakage prior to administration.

Missed dose:

If you forget to take your tablets you should take your next dose as usual. Do not take extra tablets to make up for the missed dose.

Side Effects

Along with its intended action, any medication may cause unwanted effects. However, check with your doctor or pharmacist promptly if any of the following persist or become troublesome:

  • nausea (feeling sick),

  • vomiting (being sick) and

  • diarrhoea

If the injection is given too quickly, you can feel dizzy due to reduced blood pressure.

Warnings and Precautions

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

  • you have kidney disease. The medicine can accumulate in your body. Therefore a lower dose might be given to you.

  • you have bleeding from the upper urinary tract. This shows as blood in your urine.

  • you have ever had any uncontrollable bleeding (including irregular menstrual bleeding).

  • you are pregnant or breastfeeding.

  • you are taking “the pill” (hormonal contraceptives) or anticoagulants (drugs to inhibit blood from clotting as much).

  • you are being treated for disseminated intravascular coagulation CYKLOKAPRON will only be given if your doctor has done blood tests to check you are suitable, otherwise other anti-clotting medicines may be a better option for you.

  • you are obese, diabetic, have been told you have polycystic ovary syndrome a history of cancer of the endometrium in a close relative, are on estrogen therapy or are taking tamoxifen.

Tell your doctor or pharmacists about any prescription and non-prescription medicines you are taking, including natural or herbal remedies.

CYKLOKAPRON is not recommended for children under 18 years of age with abnormally heavy menstrual flow (hypermenorrhea).

CYKLOKAPRON may cause disturbance to your colour vision. If you are to be treated for several weeks with CYKLOKAPRON, it is advisable to have an eye check up (for sharpness of vision, colour vision, field of vision etc.) before you start on CYKLOKAPRON and at regular intervals. If you notice any change in your vision, especially in your colour vision, tell your doctor or pharmacist right away so that they can arrange for you to safely stop taking CYKLOKAPRON.

If you are taking CYKLOKAPRON for heavy periods, you should monitor your menstrual flow. If menstrual bleeding is not reduced after three menstrual cycles, consult with your doctor, an alternative treatment may be necessary.

If you experience (feel) dizziness, do not drive or use machinery.

Interactions with this medication

Tell your doctor or pharmacist about any medicines you use including any prescription, over the counter or natural health products.

Drugs that may interact with CYKLOKAPRON include:

  • any medicines used to help your blood clot.

  • medicines that decrease blood clots (anticoagulants). Treatment with anticoagulants must take place under the strict supervision of a physician experienced in this field.

  • birth control that contains hormones such as “The Pill”. The Pill along with CYKLOKAPRON may increase your chance of having a blood clot, stroke, or heart attack.

  • hydrochlorothiazide, desmopressin, sulbactam-ampicillin, carbazochrome, ranitidine, or nitroglycerin. These medicines along with CYKLOKAPRON may lead to heart attacks.

Other related products

Cyclomen (Danazol)

Author , posted on July 2, 2017

Category:


Cyclomen

Danazol

Select Quantity:
Select Quantity:
Select Quantity:

Cyclomen (Danazol) Medication Information

 

Uses

Cyclomen is used to treat:

  • Treatment of endometriosis 
  • Symptoms of fibrocystic breast disease associated with severe breast pain and tenderness

Dosage

The oral capsules are available in the following strengths:

  • 50 mg
  • 100 mg
  • 200 mg

Side Effects

The most common side effects of Cyclomen include:

  • Development of male characteristics
  • Headache
  • Change in vision
  • Loss of appetite
  • Nausea
  • Vomiting
  • Blood clot
  • Jaundice 

To obtain a full list of side effects that apply to you, contact your doctor or pharmacist

Precautions

Cyclomen can cause harm to an unborn baby when given to pregnant women.

The use of Cyclomen to treat endometriosis may increase the risk of cancer of the ovaries or may induce tumors of the liver.

Interactions

Common medications that interact with Cyclomen are listed:

  • Carbamazepine
  • Phenytoin
  • Cyclosporine
  • Tacrolimus
  • Anti-hypertensive
  • Insulin
  • Statins
  • Warfarin 

Contact your doctor or pharmacist to receive more information

Storage

Store at controlled room temperature (68-77ºF). Keep out of reach of children.

Pharmacist Tips

  • If you miss a dose of Cyclomen, you should take it as soon as possible, unless it is already time for your next dose. Then skip the missed dose and take the regularly scheduled dose to avoid double doses
  • If suspected of a drug overdose, even when no symptoms present, immediately contact your doctor, emergency department or regional Poison Control Center
  • If your symptoms return after finishing treatment with Cyclomen, talk to your doctor to discuss if you may be able to start the treatment again

Danazol FAQs

Should this be given with food?

Can be given with or without food

 

What is the length of treatment?

Recommended time for treatment is a maximum of three to six months

 

Should I use birth control while on this medication?

An effective non-hormonal method of contraception should be used during the complete course of therapy.

 

Can irregular periods occur with this medication?

Regular menstrual patterns, irregular menstrual patterns, and amenorrhea each occur in approximately one-third of patients treated with 100 mg of Cyclomen. However, these are observed more often with higher doses. 

 

What is the drug danazol used for?

Cyclomen is used to treat cyclic breast pain, as well as endometriosis. 

 

Is danazol a steroid?

Cyclomen is not a steroid. 

 

What is the mechanism of action of danazol?

Cyclomen suppresses the body’s release of follicle-stimulating hormone and luteinizing hormone, to decrease the rate of growth of abnormal breast tissue, and to reduce the amount of tissue in the uterus.

 

Does danazol increase testosterone?

Danazol increases the concentration and proportion of testosterone that is carried unbound in the blood. 

 

Related Drugs

  • Aygestin
  • Deblitane
  • Errin
  • Lyleq
  • Lyza
  • Norlyroc

Reference:

Cyclomen {package insert}. Laval, Quebec: Sanofi-Aventis Canada Inc.; 2017.

https://products.sanofi.ca/en/Cyclomen.pdf

PharmD Medical Writer

Author: Dr. Larisa Roybal, PharmD

Dr. Roybal is a board-certified pharmacotherapy specialist who has practiced in both ambulatory and acute care settings. Her pharmacy interests include oncology and general inpatient pharmacy.