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Topiramate Cadila 200 mg film-coated tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) ▼ Additional monitoring Details

Medicine strength:
200 mg
Contains active substance:
ATC code:

Patient leaflet - Topiramate Cadila 200 mg film-coated tablets

1. WHAT TOPIRAMATE TABLETS ARE AND WHAT THEY ARE USED FOR

Topiramate Tablets belong to a group of medicines called “antiepileptic medicines”. They can be used:

  • alone to treat seizures in adults and children over age 6
  • with other medicines to treat seizures in adults and children over age 2
  • to prevent migraine headaches in adults

2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE TOPIRAMATE TABLETS

Do not take Topiramate Tablets:

if you are allergic (hypersensitive) to topiramate, or any of the other ingredients in Topiramate Tablets (listed in section 6).

Migraine prevention

  • You must not use Topiramate Tablets if you are pregnant.
  • If you are a woman who is able to become pregnant, you must not take Topiramate Tablets unless you use highly effective contraception (birth control) during your treatment. See below under “Pregnancy, breast-feeding and fertility – Important advice for women”.

Treatment of epilepsy

  • You must not use Topiramate Tablets if you are pregnant, unless no other treatment gives sufficient seizure control for you.
  • If you are a woman who is able to become pregnant, you must not take Topiramate Tablets unless you use highly effective contraception (birth control) during your treatment. Do not stop taking Topiramate Tablets or your contraception until you have discussed this with your doctor. Your doctor will advise you further and make sure you are aware of and understand all of the risks of taking Topiramate Tablets during pregnancy and the risks of seizures during pregnancy. See below under “Pregnancy, breast-feeding and fertility – Important advice for women”.

Make sure you read the patient guide that you will receive from your doctor.

A patient card is provided with the Topiramate package to remind you of the risks in pregnancy.

If you are not sure if the above applies to you, talk to your doctor or pharmacist before using Topiramate Tablets.

Warnings and precautions

Talk to your doctor or pharmacist before taking Topiramate Tablets if you:

  • have kidney problems, especially kidney stones or are getting kidney dialysis
  • have a history of blood and body fluid abnormality (metabolic acidosis)
  • have liver problems
  • have eye problems, especially glaucoma
  • have a growth problem
  • are on a high fat diet (ketogenic diet)
  • are a woman who is able to become pregnant. Topiramate Tablets can harm an unborn child when taken during pregnancy. Highly effective contraception (birth control) must be used during your treatment and for at least 4 weeks after the last Topiramate dose. See section ‘pregnancy and breastfeeding’ for further information.
  • are pregnant. Topiramate Tablets can harm an unborn child when taken during pregnancy.

If you are not sure if any of the above apply to you, talk to your doctor before using Topiramate Tablets.

If you have epilepsy, it is important that you do not stop taking your medicine without first consulting your doctor.

You should also talk to your doctor before taking any medicine containing topiramate that is given to you as an alternative to Topiramate Tablets.

You may lose weight if you use Topiramate Tablets so your weight should be checked regularly when using this medicine. If you are losing too much weight or a child using this medicine is not gaining enough weight, you should consult your doctor.

A small number of people being treated with anti-epileptic medicines such as Topiramate Tablets have had thoughts of harming or killing themselves. If at any time you have these thoughts, immediately contact your doctor.

Topiramate Tablets may in rare cases cause high levels of ammonia in the blood (seen in blood tests) which can lead to a change in brain function, especially if you are also taking a medicine called valproic acid or sodium valproate. Since this may be a severe condition, tell your doctor immediately if the following symptoms occur (see also section 4 ‘Possible side effects’):

  • difficulty thinking, remembering information, or solving problems
  • being less alert or aware
  • feeling very sleepy with low energy

At higher doses of Topiramate Tablets, the risk of developing these symptoms may increase.

Other medicines and Topiramate Tablets

Please tell your doctor or pharmacist if you are taking or have recently taken or might take any other medicines. Topiramate Tablets and certain other medicines can affect each other. Sometimes the dose of some of your other medicines or Topiramate Tablets will have to be adjusted.

Especially tell your doctor or pharmacist if you are taking:

  • other medicines that impair or decrease your thinking, concentration or muscle co-ordination (e.g. central nervous system depressant medicines such as muscle relaxants and sedatives)
  • hormonal contraceptives. Topiramate can affect how well some hormonal contraceptive (birth control) methods work. An additional barrier method of contraception such as a condom or pessary/diaphragm should be used. You should talk to your doctor about the best kind of contraception to use while you are taking Topiramate Tablets.

Tell your doctor if your menstrual bleeding changes while you are taking hormonal contraceptives and Topiramate Tablets. Irregular bleeding may occur. In this case, continue taking the hormonal contraceptives and inform your doctor.

Keep a list of all the medicines you take. Show this list to your doctor and pharmacist before you start a new medicine.

Other medicines you should discuss with your doctor or pharmacist include other anti-epileptic medicines, risperidone, lithium, hydrochlorothiazide, metformin, pioglitazone, glyburide, amitriptyline, propranolol, diltiazem, venlafaxine, flunarazine St. John's wort (Hypericum perforatum) (a herbal preparation used to treat depression), warfarin used to thin the blood.

If you are not sure if any of the above applies to you, talk to your doctor or pharmacist before you start a new medicine.

Topiramate Tablets with food and drink

Topiramate Tablets can be taken with or without food. Drink plenty of fluids during the day to prevent kidney stones while taking Topiramate Tablets. You should avoid drinking alcohol while taking Topiramate Tablets.

Pregnancy, breast-feeding and fertility

Important advice for women who are able to become pregnant

Topiramate Tablets can harm an unborn child. If you are a woman who is able to become pregnant, talk to your doctor about other possible treatments. Visit your doctor to review your treatment and discuss the risks at least once a year.

Migraine prevention:

  • For migraine, you must not use Topiramate Tablets if you are pregnant.
  • For migraine, you must not use Topiramate Tablets if you are a woman who is able to become pregnant unless you are using highly effective contraception (birth control).
  • Before the start of treatment with Topiramate Tablets a pregnancy test should be performed in a woman who is able to become pregnant.

Treatment of epilepsy:

  • For epilepsy, you must not use Topiramate Tablets if you are pregnant, unless you and your doctor have agreed that no other treatment gives sufficient seizure control for you.
  • For epilepsy, you must not use Topiramate Tablets if you are a woman who is able to become pregnant unless you are using highly effective contraception. Do not stop taking Topiramate Tablets or your contraception (birth control) until you have discussed this with your doctor. Your doctor will make sure you have received information about the risks of taking Topiramate Tablets during pregnancy and about the risks of seizures during pregnancy, which may put you or your unborn child at risk.
  • Before the start of treatment with Topiramate Tablets a pregnancy test should be performed in a woman who is able to become pregnant.

The risks of topiramate when taken during pregnancy. The risks apply whether topiramate is taken for migraine prevention or treatment of epilepsy.

There is a risk of harm to the unborn child if Topiramate Tablets is used during pregnancy.

  • If you take Topiramate Tablets during pregnancy, your child has a higher risk for birth defects. In women who take topiramate, around 4 - 9 children in every 100 will have birth defects. This compares to 1-3 children in every 100 born to women who do not have epilepsy and do not take an antiepileptic treatment. Particularly, cleft lip (split in the top lip) and cleft palate (split in the roof of the mouth) have been observed. Newborn boys may also have a malformation of the penis (hypospadia). These defects can develop early in pregnancy, even before you know you are pregnant.
  • If you take Topiramate Tablets during pregnancy, your child may have a 2- to 3-fold higher risk for autism spectrum disorders, intellectual disabilities, or attention deficit hyperactivity disorder (ADHD) compared with children born to women with epilepsy not taking antiepileptic medication.
  • If you take Topiramate Tablets during pregnancy, your child may be smaller and weigh less than expected at birth. In one study, around 18 in every 100 children of mothers taking topiramate during pregnancy were smaller and weighed less than expected at birth, while around 5 in every 100 children born to women without epilepsy and not taking antiepileptic medication were smaller and weighed less than expected at birth.
  • Talk to your doctor if you have questions about this risk during pregnancy.
  • There may be other medicines to treat your condition that have a lower risk of birth defects.

Need for contraception (birth control) in women who are able to become pregnant:

  • If you are a woman who is able to become pregnant, talk to your doctor about other possible treatments instead of Topiramate Tablets. If the decision is made to use Topiramate Tablets you must use highly effective contraception during your treatment and for at least 4 weeks after the last Topiramate Tablets dose.
  • One highly effective contraception (such as an intrauterine device) or two complementary contraceptives such as birth control pill together with a barrier method of birth control (such as a condom or pessary/diaphragm) must be used. Talk to your doctor about what contraception is most appropriate for you.
  • Topiramate can affect how well some hormonal contraceptive (birth control) methods work. If you are taking hormonal contraceptives, an additional barrier contraceptive method (such as a condom or pessary/diaphragm) should be used.
  • Tell your doctor if you experience irregular menstrual bleeding.

Use of Topiramate Tablets in girls:

If you are a parent or a caregiver of a girl treated with Topiramate Tablets, you must contact her doctor immediately once your child experiences her first period (menarche). The doctor will inform you about the risks to an unborn child due to topiramate exposure during pregnancy, and the need for using highly effective contraception.

If you wish to become pregnant while taking Topiramate Tablets:

  • Schedule an appointment with your doctor.
  • Do not stop using your contraception until you have discussed this with your doctor.
  • If you take Topiramate Tablets for epilepsy, do not stop taking it until you have discussed this with your doctor. Suddenly stopping Topiramate Tablets can cause seizures to start again or happen more often or last longer than before. This may put you or your unborn child at risk.
  • Your doctor will reassess your treatment as they may need to change or stop your medicine. The doctor will counsel you about the risks of Topiramate Tablets during pregnancy. He/she may also refer you to another specialist.

If you have become pregnant or think you may be pregnant while taking Topiramate Tablets:

  • Schedule an urgent appointment with your doctor.
  • If you are taking Topiramate Tablets to prevent migraine, stop taking the medicine straight away, and contact your doctor. Your doctor will assess your condition and discuss your options with you.
  • If you are taking Topiramate Tablets for epilepsy, do not stop taking this medicine unless your doctor tells you to. Suddenly stopping Topiramate Tablets can cause seizures to start again or happen more often or last longer than before. This may put you or your unborn child at risk.
  • If you are taking Topiramate Tablets for epilepsy, your doctor will assess your condition and discuss options with you. Your doctor will make sure you are aware of and understand all the risks of Topiramate Tablets during pregnancy. They may advise that you need to switch to another medicine to treat your epilepsy. If so, they will explain how to make the change to this new medicine. He/she may also refer you to another specialist.
  • If Topiramate Tablets is used during pregnancy for epilepsy, you will be monitored closely to check how your unborn child is developing.

Make sure you read the patient guide that you will receive from your doctor.

A patient card is provided with the Topiramate package to remind you of topiramate risks in pregnancy.

Breast-feeding

The active substance in Topiramate Tablets (topiramate) passes into human milk. Effects have been seen in breastfed babies of treated mothers, including diarrhoea, feeling sleepy, feeling irritable, and poor weight gain. Therefore, your doctor will discuss with you whether you abstain from breast-feeding or whether to abstain from treatment with Topiramate Tablets. Your doctor will take into account the importance of the medicine to the mother and the risk for the baby.

Mothers who breast-feed while taking Topiramate Tablets must tell their doctor as soon as possible if the baby experiences anything unusual.

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Package leaflet: Information for the patient

TOPIRAMATE CADILA 25 mg, 50 mg, 100 mg and 200 mg FILM-COATED TABLETS (topiramate)

TOPIRAMATE CADILA

25 mg, 50 mg, 100 mg and 200 mg

FILM-COATED TABLETS

OETEC1560

TOPIRAMATE CADILA

25 mg, 50 mg, 100 mg and 200 mg

FILM-COATED TABLETS

OETEC1560

Product

Substrate:

Market

Mfg. Location

Component Change part Layout:

TOPIRAMATE

OETEC1560 Dholka

Export (Novumgen Cubic UK)

leaflet - Front Side

240 x 485 mm

NA

28 gsm Bible paper printed pack insert (Folding size: 40 x 70 mm) with patient card pasted through perforated Tape

C A D IL A PH A R MA C E U T IC A L S LT D .

Driving and using machines

Dizziness, tiredness and vision problems may occur during treatment with Topiramate Tablets. Do not drive or use any tools or machines without talking to your doctor first.

Topiramate Tablets contains lactose.

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

3. HOW TO TAKE TOPIRAMATE TABLETS

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

  • Your doctor will usually start you on a low dose of topiramate and slowly increase your dose until the best dose is found for you.
  • Topiramate Tablets are to be swallowed whole. Avoid chewing the tablets as they may leave a bitter taste.
  • Topiramate Tablets can be taken before, during, or after a meal. Drink plenty of fluids during the day to prevent kidney stones while taking topiramate.

If you take more Topiramate Tablets than you should

  • See a doctor right away. Take the medicine pack with you.
  • You may feel sleepy, tired, or less alert; lack coordination; have difficulty speaking or concentrating; have double or blurred vision; feel dizzy due to low blood pressure; feel depressed or agitated; or have abdominal pain, or seizures (fits).

Overdose can happen if you are taking other medicines together with Topiramate Tablets.

If you forget to take Topiramate Tablets

  • If you forget to take a dose, take it as soon as you remember it. However, if it is almost time for your next dose, skip the missed dose and continue as usual. If you miss two or more doses, contact your doctor.
  • Do not take a double dose (two doses at the same time) to make up for a forgotten dose.

If you stop taking Topiramate Tablets

Do not stop taking this medicine unless told to do so by your doctor. Your symptoms may return. If your doctor decides to stop this medication, your dose may be decreased gradually over a few days.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS

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

Tell your doctor, or seek medical attention immediately if you have the following side effects: Very common (may affect more than 1 in 10 people):

  • depression (new or worse)

Common (may affect up to 1 in 10 people):

  • Seizures (fits)
  • Anxiety, irritability, changes in mood, confusion, disorientation
  • Problems with concentration, slowness of thinking, loss of memory, problems with memory (new onset, sudden change or increased severity)
  • Kidney stone, frequent or painful urination

Uncommon (may affect up to 1 in 100 people):

  • Increased acid level in the blood (may cause troubled breathing including shortness of breath, loss of appetite, nausea, vomiting, excessive tiredness, and fast or uneven heart beats)
  • Decreased or loss of sweating (particularly in young children who are exposed to high temperatures)
  • Having thoughts of serious self-harm, trying to cause serious self-harm
  • Loss of part of the field of vision

Rare (may affect up to 1 in 1,000 people):

  • Stevens Johnson syndrome, a potentially life-threatening condition that may present with sores in multiple mucosal sites (such as the mouth, nose, and eyes), a skin rash, and blistering.
  • Glaucoma – blockage of fluid in eye causing increased pressure in the eye, pain, or decreased vision
  • Difficulty thinking, remembering information, or solving problems, being less alert or aware, feeling very sleepy with low energy – these symptoms may be a sign of a high level of ammonia in the blood (hyperammonemia), which can lead to a change in brain function (hyperammonemic encephalopathy).

Not known: frequency cannot be estimated from the available data:

  • Toxic epidermal necrosis, a life-threatening condition related to, yet more severe than, Stevens-Johnson syndrome, characterized by widespread blistering and sloughing of the outer layers of the skin (see rare side effects).
  • Inflammation of the eye (uveitis) with symptoms such as eye redness, pain, sensitivity to light, runny eyes, seeing small dots or getting blurred vision

Other side effects include the following, if they get serious, please tell your doctor or pharmacist:

Very common (may affect more than 1 in 10 people)

  • Stuffy, runny nose or sore throat
  • Tingling, pain and/or numbness of various body parts
  • Sleepiness, tiredness
  • Dizziness
  • Nausea, diarrhoea
  • Weight loss

Common (may affect up to 1 in 10 people)

  • Anaemia (low blood count)
  • Allergic reaction (such as skin rash, redness, itching, facial swelling, hives)
  • Loss of appetite, decreased appetite
  • Aggression, agitation, anger, abnormal behaviour
  • Difficulty falling or staying asleep
  • Problems with speech or speech disorder, slurred speech
  • Clumsiness or lack of coordination, feeling of unsteadiness when walking
  • Decreased ability to complete routine tasks
  • Decreased, loss of, or no sense of taste
  • Involuntary trembling or shaking; rapid, uncontrollable movements of the eyes
  • Visual disturbance, such as double vision, blurred vision, decreased vision, difficulty focusing
  • Sensation of spinning (vertigo), ringing in the ears, ear pain
  • Shortness of breath
  • Cough
  • Nose bleeds
  • Fever, not feeling well, weakness
  • Vomiting, constipation, abdominal pain or discomfort, indigestion, stomach or intestinal infection
  • Dry mouth
  • Hair loss
  • Itching
  • Joint pain or swelling, muscle spasms or twitching, muscle aches or weakness, chest pain
  • Weight gain

Uncommon (may affect up to 1 in 100 people)

  • Decrease in platelets (blood cells that help stop bleeding), decrease in white blood cells that help to protect you against infection, decrease in potassium level in the blood
  • Increase in liver enzymes, increase in eosinophils (a type of white blood cell) in the blood
  • Swollen glands in the neck, armpit, or groin
  • Increased appetite
  • Elevated mood
  • Hearing, seeing, or feeling things that are not there, severe mental disorder (psychosis)
  • Showing and/or feeling no emotion, unusual suspiciousness, panic attack
  • Problems with reading, speech disorder, problems with handwriting
  • Restlessness, hyperactivity
  • Slowed thinking, decreased wakefulness or alertness
  • Reduced or slow body movements, involuntary abnormal or repetitive muscle movements
  • Fainting
  • Abnormal sense of touch; impaired sense of touch
  • Impaired, distorted, or no sense of smell
  • Unusual feeling or sensation that may precede a migraine or a certain type of seizure
  • Dry eye, sensitivity of the eyes to light, eyelid twitching, watery eyes
  • Decreased or loss of hearing, loss of hearing in one ear

    • Slow or irregular heartbeat, feeling your heart beating in your chest
    • Low blood pressure, low blood pressure upon standing (consequently, some people taking Topiramate Tablets may feel faint, dizzy, or may pass out when they stand up or sit up suddenly)
    • Flushing, feeling warm
    • Pancreatitis (inflammation of the pancreas)
    • Excessive passing of gas or wind, heartburn, abdominal fullness or bloating
    • Bleeding gums, increased saliva, drooling, breath odour
    • Excessive intake of fluids, thirst
    • Skin discolouration
    • Muscle stiffness, pain in side
    • Blood in urine, incontinence (lack of control) of urine, urgent desire to urinate, flank or kidney pain
    • Difficulty getting or keeping an erection, sexual dysfunction
    • Flu-like symptoms
    • Cold fingers and toes
    • Feeling drunk
    • Learning disability

Rare (may affect up to 1 in 1,000 people)

  • Abnormally elevated mood
  • Loss of consciousness
  • Blindness in one eye, temporary blindness, night blindness
  • Lazy eye
  • Swelling in and around the eyes
  • Numbness, tingling and colour change (white, blue then red) in fingers and toes when exposed to the cold
  • Inflammation of the liver, liver failure
  • Abnormal skin odour
  • Discomfort in your arms or legs
  • Kidney disorder

Not known (frequency cannot be estimated from the available data)

  • Maculopathy is a disease of the macula, the small spot in the retina where vision is keenest. You should call your doctor if you notice a change or decrease in your vision.

Children

The side effects in children are generally similar to those seen in adults, but the following side effects may be more common in children than adults:

  • Problems with concentration
  • Increased acid level in the blood
  • Having thoughts of serious self-harm
  • Tiredness
  • Decreased or increased appetite
  • Aggression, abnormal behaviour
  • Difficulty falling or staying asleep
  • Feeling of unsteadiness when walking
  • Not feeling well
  • Decrease in potassium level in the blood
  • Showing and/or feeling no emotion
  • Watery eyes
  • Slow or irregular heartbeat

Other side effects that may occur in children are:

Common (may affect up to 1 in 10 people)

  • Sensation of spinning (vertigo)
  • Vomiting
  • Fever

Uncommon (may affect up to 1 in 100 people)

  • Increase in eosinophils (a type of white blood cell) in the blood
  • Hyperactivity
  • Feeling warm
  • Learning disability

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk /yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE TOPIRAMATE TABLETS

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the carton after (Exp.). The expiry date refers to the last day of that month.

This medicinal product does not require any special storage conditions. Store in the original package. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. CONTENTS OF THE PACK AND OTHER INFORMATION

What Topiramate Tablets contain:

The active substance is topiramate.

Each film-coated tablet contains 25 mg, 50 mg, 100 mg or 200 mg of topiramate.

Tablet core:

The ingredients are lactose monohydrate, pregelatinized starch, microcrystalline cellulose, sodium starch glycolate and magnesium stearate.

Film-coating:

Topiramate 25 mg Tablets are coated with the ingredients of titanium dioxide, hypromellose, polysorbate 80 and indigo carmine aluminium lake (E132).

Topiramate 50 & 100 mg Tablets are coated with the ingredients of titanium dioxide, hypromellose, polysorbate 80, iron oxide yellow (E172) and iron oxide red (E172).

Topiramate 200 mg Tablets are coated with the ingredients of titanium dioxide, hypromellose, polysorbate 80 and iron oxide red (E172).

What Topiramate Tablets look like and the contents of the pack:

Topiramate 25 mg: white coloured, circular, biconvex film-coated tablets.

Topiramate 50 mg: light-orange coloured, circular, biconvex film-coated tablets. Topiramate 100 mg: orange coloured, circular, biconvex film-coated tablets.

Topiramate 200 mg: pink coloured, biconvex, caplet-shaped film-coated tablets. Topiramate Tablets are available in containers of 60, 100 & 200 film-coated tablets and blister packs of 28, 56, 60 & 84 film-coated tablets. Not all pack sizes may be marketed.

Marketing Authorisation Holder:

Cadila Pharmaceuticals (UK) Limited

Amba House 4th Floor,

Kings Suite 15 College Road,

Harrow, Middlesex,

HA1 1BA, United Kingdom

Manufacturer:

Cubic Pharmaceuticals Limited,

Unit 3, Sextant Park, Neptune Close, Medway City Estate,

Rochester, ME2 4LU, United Kingdom.

Distributor:

Novumgen Limited

G34, Suite F,

Breakspear Park, Breakspear Way

Hemel Hempstead,

HP2 4TZ, United Kingdom

This leaflet was last revised in June 2024.

5 mm

5 mm

240 mm

Product

Substrate:

Market

Mfg. Location

Component Change part Layout:

TOPIRAMATE

OETEC1560 Dholka

Export (Novumgen Cubic UK)

leaflet - Back Side

240 x 485 mm

NA

28 gsm Bible paper printed pack insert (Folding size: 40 x 70 mm) with patient card pasted through perforated Tape

C A D IL A PH A R MA C E U T IC A L S LT D .

BS-05/07/24-V03 BS-01/07/24-V02 BS-28/03/24-V01 Product

Substrate:

Market

Mfg. Location

Component Change part Layout:

TOPIRAMATE

OETEC1560 Dholka

Export (Novumgen Cubic UK)

leaflet - Front Side

240 x 485 mm

NA

28 gsm Bible paper printed pack insert (Folding size: 40 x 70 mm) with patient card pasted through perforated Tape

C A D IL A PH A R MA C E U T IC A L S LT D .

BS-05/07/24-V03 BS-01/07/24-V02 BS-28/03/24-V01 Topiramate▼

Pregnancy Prevention

Programme

Patient Card

Topiramate Cadila 25 mg

Topiramate Cadila 50 mg

Topiramate Cadila 100 mg

Topiramate Cadila 200 mg

Size : 160 x 70 mm Folding Size: 70 x 40 Color : Black

Front

PRESCRIBING DOCTOR’S NAME:

PRESCRIBING DOCTOR’S PHONE NUMBER:

Size : 160 x 70 mm

Folding Size: 70 x 40 Color : Black

Back

OETEC1560 •Topiramate is an effective medicine for epilepsy and prevention of migraine.

  • Topiramate can seriously harm a baby when taken during pregnancy.
  • Use effective birth control (contraception) at all times during your treatment with topiramate and for at least 4 weeks after the last dose.
  • Discuss with your doctor about which method of birth control is most suitable for you.
  • It is important to visit your doctor to review your treatment at least once each year.

    What you must do

    • Read the package leaflet carefully before use.
    • Read the Patient Guide for the topiramate pregnancy prevention programme. You should have received a copy from your doctor or it can be found online at www.medicines.org.uk by entering “topiramate” in the search box and then clicking on “Risk Materials”.
    • If you are thinking about having a baby, make an appointment with your GP. Do not stop using topiramate and contraception before you have talked to your doctor.

▼ This medicinal product is subject to additional monitoring. Report any side

effects to

www.mhra.gov.uk/ yellowcard or search for MHRA Yellow Card in the

Google Play or Apple

App Store.

Important information for all patients who could become pregnant

Contraception and Pregnancy

Prevention – Important information to know

  • If you think you are pregnant and are taking topiramate for epilepsy, do not stop using topiramate. This may cause your seizures to start again or happen more often and last longer. Make an urgent appointment with your GP or epilepsy team (within a few days).
  • If you think you are pregnant and are taking topiramate for migraine prevention, stop taking topiramate straight away and contact your GP.

Product

Substrate:

Market

Mfg. Location

Component Change part Layout:

TOPIRAMATE

OETEC1560 Dholka

Export (Novumgen Cubic UK)

leaflet - Front Side

240 x 485 mm

NA

28 gsm Bible paper printed pack insert (Folding size: 40 x 70 mm) with patient card pasted through perforated Tape

C A D IL A PH A R MA C E U T IC A L S LT D .

BS-05/07/24-V03 BS-01/07/24-V02 BS-28/03/24-V01

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 45841/0022

Last revision stated in the text: June 2024 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Topiramate Cadila 200 mg film-coated tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Topiramate
Strength 200 mg
Pharmaceutical form Oral tablet
How is it taken Oral
Excipients Pre-gelatinised Starch (PA 5PH), Lactose monohydrate, Microcrystalline cellulose (Avicel PH 101), Sodium starch glycolate (Type A), Magnesium stearate, Titanium dioxide, Hypromellose, PEG 400, Polysorbate 80, Iron oxide red
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life Blister - 3 years
Bottles - 2 years
Storage This medicinal product does not require any special storage conditions.
Store in the original package.
Drug group (ATC) Antiepileptics, other antiepileptics, antimigraine preparations
  1. N Nervous system drugs
    1. N03 Antiepileptics
      1. N03A Antiepileptics
        1. N03AX Other antiepileptics
          1. N03AX11 topiramate
Additional monitoring Yes ▼ – new safety information is collected quickly. Report any side effect to the Yellow Card scheme.
Marketing authorisation PL 45841/0022 (first authorised 17 December 2024)
Marketing authorisation holder Cadila Pharmaceuticals (UK) Limited
Codes BNF 04080100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.