BETASERC
PolandIt is used in the treatment of Ménière's disease (manifesting as dizziness with nausea or vomiting, progressive hearing loss, and tinnitus) and for the symptomatic treatment of vestibular vertigo.
Frequently asked questions
How should Betaserc be used?
The tablets should be swallowed with water. They can be taken with or without food; however, taking them with a meal may help reduce potential gastrointestinal discomfort. In the case of an 8 mg dose, one or two tablets are usually taken three times a day, distributed evenly throughout the day and attempting to take them at regular times.
When should you not take this medicine?
Do not use it if you are allergic to betahistine or any other ingredients of the medicine, or if a pheochromocytoma of the adrenal gland has been diagnosed in the patient. The medicine is also not recommended for persons under 18 years of age.
Can this medicine be used with other preparations?
You should inform your doctor about all medicines you are taking, especially antihistamines (which may affect the efficacy of the preparation in both directions) and monoamine oxidase inhibitors (MAOIs), which are used in the treatment of depression or Parkinson's disease and may enhance the effect of the medicine.
What are the possible side effects of Betaserc?
Nausea, headaches, and digestive disorders may occur frequently. Mild gastrointestinal complaints such as vomiting, abdominal pain, intestinal pain, bloating, and gas may also occur. You must immediately discontinue use and contact a doctor if an allergic reaction occurs (e.g., rash, facial swelling, difficulty breathing, loss of consciousness).
Can the medicine be used during pregnancy or breastfeeding?
In the case of pregnancy, the medicine should only be taken if a doctor deems it necessary; if you suspect you are pregnant, discontinue use and inform your doctor. During breastfeeding, the medicine should not be used unless approved by a doctor.
Instructions for use
Package leaflet: Information for the patient
Warning! Keep this leaflet. The information on the immediate packaging is in a foreign language.
Betaserc
8 mg, tablets
Betahistini dihydrochloridum
Please read this leaflet carefully before taking the medicine, as it contains
important information for the patient.
- Keep this leaflet, as you may need to read it again.
- Consult your doctor, pharmacist, or nurse if you have any doubts.
- This medicine has been prescribed for a specific individual. Do not pass it on to others. The medicine may harm someone else, even if their symptoms are the same.
- If any adverse reactions occur, including any possible adverse reactions not listed in this leaflet, inform your doctor, pharmacist, or nurse. See section 4.
Table of contents of the leaflet
- What Betaserc is and what it is used for
- Important information before taking Betaserc
- How to take Betaserc
- Possible side effects
- How to store Betaserc
- Contents of the pack and other information
1. What Betaserc is and what it is used for
What Betaserc is
Betaserc contains betahistine. Betaserc is a type of medicine known as a "histamine analogue".
What Betaserc is used for
Betaserc is used in the treatment of Ménière's disease, which is characterized by the following
symptoms:
- vertigo (with nausea, vomiting),
- progressive hearing loss,
- tinnitus.
Also used in symptomatic treatment of vestibular-origin dizziness.
How Betaserc works
Betaserc works by improving blood flow in the inner ear. This leads to a reduction in elevated
pressure.
2. Important information before taking Betaserc
When not to take Betaserc
- if the patient is allergic (hypersensitive) to betahistine or any of the other ingredients of Betaserc (listed in section 6),
- if the patient has been diagnosed with a tumour of the adrenal gland (‘phaeochromocytoma’).
Do not take Betaserc if any of the above apply. If in doubt, speak to your doctor or pharmacist before taking Betaserc.
Warnings and precautions
Before taking Betaserc, consult your doctor or pharmacist if:
- the patient has ever had stomach ulcers,
- the patient suffers from bronchial asthma.
If any of the above apply (or if you have any doubts), speak to your doctor or pharmacist before taking Betaserc. Your doctor may wish to monitor the patient closely during treatment with Betaserc.
Children
Betaserc is not recommended for use in individuals under 18 years of age.
Other medicines and Betaserc
Tell your doctor or pharmacist about all medicines currently or recently taken, including those obtained without a prescription and herbal medicines.
In particular, inform your doctor or pharmacist if the patient is taking any of the following medicines:
- antihistamines – these may (theoretically) affect the action of Betaserc. Betaserc may also reduce the effectiveness of antihistamine medicines.
- monoamine oxidase inhibitors (MAOIs) – used in the treatment of depression or Parkinson’s disease. These may enhance the effect of Betaserc.
If any of the above apply (or if you have any doubts), speak to your doctor or pharmacist before taking Betaserc.
Betaserc with food and drink
Betaserc may be taken with or without food. However, Betaserc may cause mild gastrointestinal discomfort (listed in section 4). Taking Betaserc with food may help reduce gastrointestinal symptoms.
Pregnancy, breastfeeding and fertility
It is unknown whether Betaserc affects the unborn child:
- Discontinue taking Betaserc and inform your doctor if the patient is pregnant or suspects she may be pregnant.
- Do not take Betaserc during pregnancy unless your doctor decides it is necessary.
It is unknown whether Betaserc passes into breast milk:
- Do not breastfeed while taking Betaserc unless your doctor authorises it.
Driving and using machines
It is unlikely that Betaserc affects the ability to drive or operate tools and machinery.
However, bear in mind that the conditions treated with betahistine (Meniere’s disease and vertigo) may cause sensations of spinning and nausea, which may affect the ability to drive and operate machinery.
3. How to take Betaserc
Always take Betaserc exactly as directed by your doctor. If you are unsure,
contact your doctor or pharmacist.
- Your doctor will adjust the dose according to your condition.
- You should continue taking the medicine. It may take some time for the medicine to start working.
How to take Betaserc
- Swallow the tablet with water.
- You may take the tablet with or without food. However, Betaserc may cause mild gastrointestinal discomfort (listed in section 4). Taking Betaserc with food may help reduce gastrointestinal discomfort.
How much Betaserc to take
Betaserc is available in two strengths: 8 mg and 24 mg. The usual dose is:
- Betaserc 8 mg – one or two tablets three times daily.
If you are taking more than one tablet per day, the doses should be evenly spaced
throughout the day, e.g., one tablet in the morning and one in the evening.
Try to take the tablets at the same times each day. This will help maintain a constant level of
medicine in your body. Taking the medicine at the same time every day will also help you remember to take it.
Taking more Betaserc than you should
If you take more Betaserc than recommended, you may experience nausea, drowsiness,
or stomach pain. If you are unsure, contact your doctor.
If you forget to take Betaserc
- If you miss a dose of Betaserc, take the next dose at your usual time.
- Do not take a double dose to make up for a missed dose.
Stopping Betaserc
Do not stop taking Betaserc without consulting your doctor, even if you feel better.
If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
4. Possible adverse reactions
Like all medicines, Betaserc may cause adverse reactions, although not everyone experiences them.
The following unwanted effects may occur after taking this medicine:
Allergic reactions
If an allergic reaction occurs, stop taking Betaserc and consult a doctor immediately or go to the nearest hospital. Symptoms may include:
- red or bumpy skin rash or inflamed skin with itching,
- swelling of the face, lips, tongue or neck,
- low blood pressure,
- loss of consciousness,
- breathing difficulties. You must stop taking Betaserc and contact a doctor immediately or go to hospital if any of the above symptoms occur.
Other adverse reactions:
Common (occurring in less than 1 in 10 people):
- nausea,
- digestive disturbances,
- headaches.
Other adverse reactions reported during treatment with Betaserc:
- Mild gastrointestinal discomfort such as vomiting, stomach and intestinal pain, bloating and gas.
Taking Betaserc with food may help reduce gastrointestinal discomfort.
Reporting of adverse reactions
If any adverse reactions occur, including those not listed in this leaflet, inform your doctor, pharmacist or nurse. Adverse reactions can also be reported directly to the Department of Monitoring Adverse Drug Reactions at the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw,
tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
Reporting adverse reactions helps provide more information on the safety of this medicine.
5. How to store Betaserc
- Keep this medicine out of sight and reach of children.
- Store at a temperature not exceeding 25°C, in a dry place.
- Do not use Betaserc after the expiry date stated on the carton and blister. The expiry date refers to the last day of the stated month.
- Medicines must not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
6. Contents of the packaging and other information
What Betaserc contains
- The active substance is 8 mg of betahistine dihydrochloride.
- The other ingredients are: microcrystalline cellulose, mannitol (E 421), citric acid monohydrate, colloidal anhydrous silica, talc.
What Betaserc looks like and contents of the pack
Betaserc 8 mg tablets are round, flat, white to almost white, with bevelled edges and a diameter of 7 mm, marked with "256" embossed on one side.
Betaserc 8 mg is available in packs of 100 tablets, packed in blisters made of PVC-PVDC/Al foil.
For further detailed information, please contact the marketing authorisation holder or the parallel importer.
Marketing authorisation holder in Romania, country of export:
Mylan Healthcare B.V.
Krijgsman 20
1186 DM Amstelveen
The Netherlands
Manufacturer:
Mylan Laboratories S.A.S.
Route de Belleville
Lieu-dit Maillard
01400 Châtillon-sur-Chalaronne
France
Parallel importer:
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Repackaged in:
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Marketing authorisation number in Romania, country of export: 2192/2009/02
Parallel import authorisation number: 80/17
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The original data is available in the language of the country of manufacture.
Data source: Register of Medicinal Products of Poland (URPL)
Data last verified: September 01, 2026