Safety and efficacy of VOTRIENT have not been established in children less than 18 years of age. VOTRIENT must not be used in children under two years of age.

BEFORE you use VOTRIENT talk to your doctor or pharmacist:

• If you have or had heart disease, heart failure or heart attack

• If you have or have had a heart rhythm disorder such as irregular heartbeat, prolongation of the QT interval or any risk factors for Torsade de Pointes (dangerous rapid fluttering of the heart) such as diabetes, low potassium, magnesium or calcium levels, or a history of low heart rate, fainting, or loss of consciousness

• If you have high blood pressure

• If you have liver disease

• If you have problems with bleeding

• If you have gastrointestinal problems

• If you have or had a blood clot in a vein or in a lung

• If you have had prior collapse of a lung

• If you have a kidney problem

• If you have thyroid problems

• If you are going to have a surgical or dental procedure, or if you have had either recently

While you are taking VOTRIENT your doctor will take blood samples to check for any liver problems. You should report any signs or symptoms of liver injury including jaundice (yellowing of whites of eyes or skin), unusual darkening of the urine, anorexia (loss of appetite), nausea, fatigue, right upper abdominal discomfort and vomiting. Your doctor will also take urine samples to check for any kidney problems. You will also have your blood pressure checked. Your doctor will periodically record your electrocardiogram (ECG) to check your heart's electrical conduction.

Your doctor will also check on any recent surgical or dental procedures to see if you are healing properly.

Use a reliable method of contraception to avoid becoming pregnant while you’re taking VOTRIENT and for up to 8 weeks after you stop treatment with VOTRIENT. If you are pregnant or think you could be, talk to your doctor about the risks and benefits to you and your baby while taking VOTRIENT. Your doctor may recommend that you don't take VOTRIENT while you are pregnant.

Breastfeeding is not recommended during treatment with VOTRIENT. Ask your doctor for advice.

Like all medicines, VOTRIENT can cause side effects.

Very common side effects—these may affect more than 1 in 10 people:

• diarrhea (which can be severe; e.g. with fever or 3 or more times a day)
• feeling or being sick (nausea or vomiting)
• loss of appetite
• stomach pain or discomfort
• high blood pressure
• headache
• loss of strength
• lack of energy
• weakness
• changes in hair colour
• weight loss
• problems with taste
• skin rash
• a skin reaction or pain on the palms of the hands or soles of the feet (including tingling, numbness, pain, swelling or reddening)
• dizziness
• cough
• shortness of breath
• chest pain
• swelling of hands, ankles or feet
• muscle pain
• pain in the bones, muscles, ligaments, joints and tendons
• mouth sores
• unusual hair loss or thinning
• loss of skin pigment
• slow heart rate

Very common side effect that may show up in your blood tests:

• increase in some substances (enzymes) produced by the liver

Common side effects—these may affect up to 1 in 10 people:

• temporary reduction in blood supply to the brain (mini-stroke)
• reduction of blood supply to the heart (angina)
• changes in the heart's electrical conduction (QT-prolongation) which may cause irregular heartbeat
• heart attack
• severe bleeding in the lung
• under-active thyroid gland
• abnormal liver function (which can be severe and may cause yellowing of the skin or the whites of the eyes (jaundice), unusual darkening of the urine, unusual tiredness, or right upper stomach area pain)
• indigestion
• flatulence
• nosebleeds
• dry skin
• nail disorder
• hoarseness
• blurred vision
• chills
• urinary tract infection
• blood in the urine
• painful urination
• sudden collapse of a lung
• heart becomes less effective at pumping blood (cardiac dysfunction)
• excessive sweating
• atypical prickling or crawling sensations on the skin
• sore mouth or mouth ulcers
• blood clot in your body (you might feel chest pain, shortness of breath, leg pain, and swelling of the legs/feet). Such blood clots can break off and travel to your lungs which may be life-threatening or even fatal
• muscle spasms

Common side effects that may show up in your blood or urine tests:

• a decrease in the number of cells involved in blood clotting (thrombocytopenia)
• low white blood cell count (neutropenia, leucopenia, lymphopenia)
• protein in urine
• increase in bilirubin (a substance produced by the liver)
• decrease in albumin (a protein found in the blood)
• increase in lipase (an enzyme from the pancreas)
• increased potassium in the blood

Uncommon side effects—these may affect up to 1 in 100 people:

• stroke
• severe bleeding in digestive tract (stomach and intestine) and brain
• a dangerous rapid fluttering of the heart (Torsades de Pointes)
• hole (perforation) in digestive tract
• abnormal connection between parts of the digestive tract (fistula)
• a sudden and severe rise in blood pressure which may be life-threatening
• liver failure

Other side effects that have occurred at an uncommon rate:

• infections, with or without changes in white blood cells (cells that fight infection)
• inflammation of the pancreas
• separation or tear of the lining of the back part of the eye (retinal detachment or tear). This can result in trouble seeing (blurry or impaired vision).

Other side effects that have occurred rarely—these may affect up to 1 in 1000 people:

• blood clots accompanied by a decrease in red blood cells and cells involved in clotting. These clots may harm organs such as the brain and kidneys.

Side Effects with Unknown Frequency:

• Interstitial lung disease, a form of lung scarring or inflammation, can have a fatal outcome in some cases. If you develop symptoms such as sudden difficulty of breathing associated with cough or fever contact your doctor immediately.
• reversible swelling in the rear part of the brain that can be associated with high blood pressure and can lead to headache, loss of speech or vision, abnormal drowsiness, confusion and/or seizure (Posterior Reversible Encephalopathy Syndrome or Reversible Posterior Leukoencephalopathy Syndrome)

Tell your doctor or pharmacist if you are taking, or have recently taken any other medicines including any medicines you bought without a prescription. This includes herbal medicines.

Some medicines may affect the way VOTRIENT works or VOTRIENT may affect how other medicines work. These include:

• clarithromycin, ketoconazole, itraconazole, telithromycin, voriconazole (used to treat infections)
• atazanavir, indinavir, nelfinavir, ritonavir, saquinavir (used to treat HIV)
• dextromethorphan (used in cough medicines)
• simvastatin and possibly other statins (used to treat high cholesterol levels)
• medicines that reduce stomach acid (e.g. esomeprazole, ranitidine, magnesium hydroxide)

Also, the following list includes some, but not all, of the drugs that may interact with VOTRIENT to affect the electrical activity of your heart:

• Antiarrhythmics (drugs that stabilize the heart rhythm function, such as quinidine, procainamide, amiodarone, sotalol, etc.)
• Antidepressants (mood disorder drugs)
• Antipsychotics (drugs used to stabilize thinking and behaviour)
• Opioids (e.g. methadone)
• Macrolide antibiotics (such as erythromycin, clarithromycin)
• Fluoroquinolone antibiotics (such as moxifloxacin, levofloxacin, ciprofloxacin)
• Antifungals (such as fluconazole, voriconazole)
• Antimalarials (e.g. quinine)
• Antinauseants (e.g. granisetron, ondansetron, dolasetron)
• Anti-asthmatics (e.g. salmeterol, formoterol)
• Tacrolimus (used after organ transplant to prevent rejection)
• Certain anticancer treatments (e.g. sunitinib, nilotinib, lapatinib, sorafenib, vorinostat)

VOTRIENT is affected by food intake. You should not drink grapefruit juice or eat grapefruit while you are being treated with VOTRIENT as this may increase the chance of side effects.

Always take VOTRIENT exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

Usual dose:

The usual dose is 800 mg VOTRIENT, taken once a day.

Do not take more than 800 mg VOTRIENT a day.

Swallow the tablets whole with water, one after the other, at about the same time each day. Do not break or crush the tablets as it affects the way the medicine is absorbed and may increase the chance of side effects.

It is important that you take VOTRIENT either at least one hour before or at least two hours after food.

Depending on your response to treatment, your doctor may recommend adjusting your dose or temporarily stopping your treatment.

Overdose:

If you have accidentally taken more VOTRIENT tablets than you should, contact your doctor, or poison control centre, or go to the emergency room of the nearest hospital even if there are no symptoms.

Missed dose:

If you forget to take VOTRIENT, do not take a double dose to make up for a missed dose. Take the next dose at the scheduled time.

XERESE is for cold sores on lips and around the mouth only. XERESE should not be used in eyes, mouth, nose, genitals, AROUND THE ANUS OR ON ANY MUCOUS MEMBRANE.

This product should not be used if you are severely immunocompromised (e.g. have HIV, cancer or are a transplant patient).

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

• Have a weak immune system (become sick very easily). It is not known if XERESE will harm you.
• Have any other medical conditions.
• Are pregnant or plan to become pregnant. It is not known if XERESE will harm your unborn baby.
• Are breast-feeding or plan to breast-feed. It is not known if XERESE is passed in your milk to your baby.

Like all medicines, XERESE can cause side effects, although not everybody gets them.

The most common side effects of XERESE are: drying or flaking of the skin, tingling or burning, redness of the skin, changes in your skin color where the cream is applied (pigmentation changes), swelling, bitter taste after you apply XERESE. If these effects become bothersome, contact your doctor.

Tell your doctor if you have any side effect that bothers you or that does not go away. These are not all the possible side effects of XERESE. For more information, ask your doctor or pharmacist.

Use XERESE exactly as directed by your doctor.

Use XERESE early, at the first sign of a cold sore (e.g. itching, burning, tingling or redness).

In case of accidental contact with the eyes or the inside of the nose or mouth, rinse thoroughly with water.

To avoid spreading the infection, do not share this medicine.

Wash your hands before and after using XERESE.

Clean and dry the skin before applying XERESE. Spread a thin layer of XERESE on the affected area.

Do not rub the cold sore because it may spread to other areas around your mouth, or make your cold sore worse.

Do not cover the cold sore or area around the cold sore with a bandage.

Do not use other skin products (such as make-up, sun screen or lip balm) or other skin medicine on the cold sore or area around the cold sore.

Do not bathe, shower or swim until 30 minutes after applying XERESE.

Talk to your doctor if your cold sore is not better in 2 weeks.

Usual adult dose:

Apply XERESE topically 5 times per day for 5 days. You should topically apply a quantity of XERESE sufficient to cover the affected area, including the outer margin. Avoid unnecessary rubbing of the affected area to avoid aggravating or transferring the infection. Wash your hands before and after the use of the cream to avoid spreading the infection.

For adolescents 12 years of age and older, the dosage is the same as in adults.

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 miss a dose of XERESE, apply it as soon as possible. However, if it is almost time for your next dose, go back to your regular dosing schedule. Do not use extra medicine to make up the missed dose.

Do not use this medication if you are allergic to ZADITOR, or if you have an untreated eye infection. ZADITOR ophthalmic should not be used to treat eye irritation caused by wearing contact lenses.

Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger amounts, or use it for longer than recommended.

If you wear contact lenses, remove them before applying ZADITOR ophthalmic. This medication may contain a preservative (benzalkonium chloride) that may cause discoloration of contact lenses. Wait at least 10 minutes after using in the eye drops before putting contact lenses into your eyes.

Do not allow the medicine dropper tip to touch any surface, including the eyes or hands. If the dropper becomes contaminated it could cause an infection in your eye, which can lead to vision loss or serious damage to the eye.

Do not use this medication if you are allergic to ZADITOR, or if you have an untreated eye infection. ZADITOR ophthalmic should not be used to treat eye irritation caused by wearing contact lenses.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment.

It is not known whether ZADITOR 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.

Do not use this medication in a child younger than 3 years old without the advice of a doctor.

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

Stop using ZADITOR ophthalmic and call your doctor at once if you have any of these serious side effects:

• redness, drainage, eyelid swelling, or other signs of infection;
• eye pain;
• vision changes; or
• severe itching of the eyes worse than before using the medication.

Less serious side effects may include:

• mild burning, stinging, or eye irritation;
• dryness of the eyes; or
• increased sensitivity to light.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect.

Avoid using other medications in your eyes during treatment with ZADITOR ophthalmic unless your doctor has told you to.

There may be other drugs that can interact with ZADITOR ophthalmic. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger amounts, or use it for longer than recommended.

Wash your hands before using the eye drops.

If you wear contact lenses, remove them before applying ZADITOR ophthalmic. This medication may contain a preservative (benzalkonium chloride) that may cause discoloration of contact lenses.

To apply the eye drops:

• Tilt your head back slightly and pull down your lower eyelid. Hold the dropper above the eye with the dropper tip down. Look up and away from the dropper as you squeeze out a drop, then close your eye. Gently press your finger to the inside corner of the eye (near your nose) for about 1 minute to keep the liquid from draining into your tear duct. If you use more than one drop in the same eye, wait about 5 minutes before putting in the next drop.

Do not allow the dropper tip to touch any surface, including the eyes or hands. If the dropper becomes contaminated it could cause an infection in your eye, which can lead to vision loss or serious damage to the eye.

After using the eyedrops, wait at least 10 minutes before putting contact lenses into your eyes.

Do not use the eye drops if the liquid has changed colors or has particles in it. Call your doctor for a new prescription.

Store the drops at room temperature away from heat and moisture. Keep the bottle tightly closed when not in use.

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

An overdose of ZADITOR ophthalmic is not expected to produce life-threatening symptoms.

Use the medication as soon as you remember the missed dose. If it is almost time for your next dose, skip the missed dose and use the medicine at your next regularly scheduled time. Do not use extra medicine to make up the missed dose.

ZANAFLEX is a short-acting medication that you should only take for daily activities that require relief from muscle spasms.

Using too much ZANAFLEX can severely damage your liver, causing liver failure.

Tell your doctor if you have any type of previous injury to your liver. Your doctor will likely check blood levels after a month of use if you fall into this category.

It's also important to inform your doctor if you have experienced kidney failure.

Call your doctor immediately if you develop dry mouth, dizziness, a strong desire for sleep, or any sign of weakness while taking ZANAFLEX. Your dosage may have to be reduced or discontinued.

You should not drive, use heavy machinery, or do any activity that requires you to be alert while using ZANAFLEX.

If you are scheduled for surgery, let your doctor know you are taking ZANAFLEX.

Before having surgery, tell your doctor or dentist about all the products you use, including over-the-counter (OTC) drugs.

In older adults, the effects of ZANAFLEX may also last much longer.

Pregnancy and ZANAFLEX

ZANAFLEX may be harmful to an unborn baby.

Animal studies have shown an adverse effect, but there are no adequate studies in pregnant women. Tell your doctor if you are pregnant or might become pregnant during treatment.

Do not use this medication without telling your doctor if you are breastfeeding.

ZANAFLEX 'High' and Recreational Use

Because of ZANAFLEX's sedative effects, numerous online and anecdotal reports have suggested that some people abuse the drug for a narcotic-like "high."

However, ZANAFLEX is not a narcotic.

ZANAFLEX has some common side effects that should go away with continued use, including:

• Dry mouth
• Weakness
• Fatigue
• Dizziness
• Nervousness
• Depression
• Vomiting
• Tingling sensation in the arms, legs, hands, and feet
• Constipation
• Diarrhea
• Stomach pain
• Heartburn
• Increased muscle spasms
• Back pain
• Rash
• Sweating
• Light-colored stools

Tell your doctor if any of these symptoms are severe or do not go away.

Serious Side Effects of ZANAFLEX

Some side effects of ZANAFLEX can be serious.

If you experience any of these symptoms, call your doctor immediately:

• Nausea
• Extreme tiredness
• Unusual bleeding or bruising
• Lack of energy
• Loss of appetite
• Pain in the upper right part of the stomach
• Yellowing of the skin or eyes (jaundice)
• Unexplained flu-like symptoms
• Seeing things or hearing voices that do not exist
• Slow heartbeat
• Changes in vision

Let your doctor know if you have any other unusual problems while taking ZANAFLEX.

Do not take ZANAFLEX if you are also taking the antidepressant fluvoxamine (Luvox) or the antibiotic ciprofloxacin (Cipro).

Let your doctor know about all other medicines and supplements you're taking before taking ZANAFLEX.

Using ZANAFLEX along with the following medicines is not recommended:

• Acyclovir (Zovirax)
• Ciprofloxacin (Cipro)
• Dronedarone (Multaq)
• Fluvoxamine (Luvox)
• Pimozide (Orap)
• Saquinavir (Invirase)
• Thioridazine (Mellaril)

Food has a complex effect on how ZANAFLEX is absorbed and processed in the body.

Starting at a lower dose and gradually increasing the dose minimizes the risk for adverse effects.

Unless your doctor tells you otherwise, continue your normal diet and take your medicine when you eat.

Alcohol and ZANAFLEX

Alcohol increases the overall amount of drug in the bloodstream.

You should not drink alcohol while taking ZANAFLEX.

ZANAFLEX also reacts differently depending on whether you take it with food or on an empty stomach, or if you sprinkle the contents of the capsule on food.

The usual starting dose is 2 mg taken by mouth every six to eight hours. A maximum of three doses can be taken in a 24-hour period. Your doctor could increase the strength in 2- to 4-mg steps to help reach the optimum effect and tolerance for your condition.

In order to reduce your risk of side effects, your doctor may direct you to start this medication at a low dose and gradually increase your dose.

Follow your doctor's instructions carefully.

ZANAFLEX Withdrawal

ZANAFLEX may cause you to have withdrawal reactions, especially if it has been used regularly for a long time or in high doses.

Withdrawal symptoms, such as anxiety, tremor, increased blood pressure, heart rate, and muscle tenseness, may occur if you suddenly stop using this medication.

To prevent this from happening, your doctor may reduce your dose gradually to discontinue your use of ZANAFLEX.

ZANAFLEX Overdose

Get immediate help or go to an emergency room if you suspect you have taken too much ZANAFLEX.

Symptoms of an overdose include:

• Blurred vision
• Chest pain
• Confusion
• Difficult or troubled breathing
• Dizziness, faintness, or lightheadedness when getting up from a lying position
• Irregular, fast or slow, or shallow breathing
• Loss of consciousness
• Pale or blue lips, fingernails, or skin
• Severe sleepiness
• Sweating

Missed Dose of ZANAFLEX

If your doctor has told you to take ZANAFLEX regularly, take the missed dose as soon as you remember it.

If it's almost time for your next dose, however, skip the missed dose and continue your regular schedule.

Don't "double up" to make up for a missed one.

ZARONTIN can cause a decrease in many types of blood cells (white cells, red cells, platelets). Call your doctor at once if you have any unusual bleeding, weakness, or any signs of infection, even if these symptoms first occur after you have been using the medication for several months.

ZARONTIN may also cause liver damage. Call your doctor if you have symptoms such as loss of appetite, stomach pain, or jaundice (yellowing of the skin or eyes).

You may have thoughts about suicide while taking this medication. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.

Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, depression, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

Do not stop using ZARONTIN without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using ZARONTIN suddenly. You will need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking ZARONTIN.

Wear a medical alert tag or carry an ID card stating that you take ZARONTIN. Any medical care provider who treats you should know that you take seizure medication.

You should not use this medication if you are allergic to ZARONTIN or to other seizure medications.

To make sure you can safely take ZARONTIN , tell your doctor if you have any of these other conditions:

• lupus;
• liver disease;
• kidney disease; or
• a history of depression, mood problems, or suicidal thoughts or actions.

You may have thoughts about suicide while taking this medication. Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed.

Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.

It is not known whether ZARONTIN is harmful to an unborn baby, but having a seizure during pregnancy could harm both mother and baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Follow your doctor's instructions about taking ZARONTIN while you are pregnant.

If you are pregnant, your name may be listed on a pregnancy registry. This is to track the outcome of the pregnancy and to evaluate any effects of ZARONTIN on the baby.

ZARONTIN passes into breast milk and could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

ZARONTIN should not be given to a child younger than 3 years old.

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.

Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, anxiety, depression, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

Call your doctor at once if you have a serious side effect such as:

• fever, chills, swollen glands, flu symptoms, sore throat, swollen glands, feeling very weak;
• new or worsening cough with fever, trouble breathing;
• easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin;
• joint pain or swelling with mild fever, muscle aches;
• chest pain, irregular heart rhythm, feeling short of breath;
• patchy skin color, red spots, or a butterfly shaped skin rash over your cheeks and nose (worsens in sunlight);
• skin rash, severe tingling, numbness, pain, muscle weakness;
• upper stomach pain, loss of appetite, dark urine, jaundice (yellowing of the skin or eyes);
• confusion, hallucinations, unusual thoughts or behavior, extreme fear;
• swelling, rapid weight gain, urinating less than usual or not at all;
• the first sign of any skin rash, no matter how mild;
• 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; or
• worsening of seizures.

Less serious side effects may include:

• upset stomach, mild nausea, stomach cramps, diarrhea, weight loss;
• swelling in your tongue or gums;
• headache, dizziness, drowsiness, feeling tired;
• lack of balance or coordination; or
• unusual vaginal bleeding.

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

Do not drink alcohol. It can increase certain side effects of ZARONTIN.

This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.

Cold or allergy medicine, sedatives, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for depression or anxiety can add to sleepiness caused by ZARONTIN. Tell your doctor if you regularly use any of these medicines, or any other seizure medication.

Before taking ZARONTIN, tell your doctor about all other seizure medications you use, especially:

• phenobarbital (Solfoton);
• phenytoin (Dilantin); or
• valproic acid (Depakene, Stavzor).

This list is not complete and other drugs may interact with ZARONTIN. 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.

Take exactly as prescribed by your doctor. Do not take in larger or smaller 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.

ZARONTIN 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. Your blood may need to be tested often. Your kidney and liver function may also need to be tested. Visit your doctor regularly.

Call your doctor at once if you have any unusual bleeding, weakness, or any signs of infection, including flu-like symptoms. These symptoms may first develop even after you have been using the medication for several months.

Do not stop using ZARONTIN without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using ZARONTIN suddenly. You may need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking ZARONTIN.

Wear a medical alert tag or carry an ID card stating that you take ZARONTIN. Any medical care provider who treats you should know that you take seizure medication.

Use ZARONTIN regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.

Store at room temperature away from moisture and heat.

Overdose symptoms may include nausea, vomiting, extreme drowsiness, and weak or shallow breathing.

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.