Betahistine Actavis 16mg Tablets

Land: Malta

Taal: Engels

Bron: Medicines Authority

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Bijsluiter Bijsluiter (PIL)
17-05-2024
Productkenmerken Productkenmerken (SPC)
17-05-2024

Werkstoffen:

BETAHISTINE DIHYDROCHLORIDE

Beschikbaar vanaf:

Actavis Group h.f. Reykjavikurvegur 78, 220 Hafnarfjörður, Iceland

ATC-code:

N07CA01

INN (Algemene Internationale Benaming):

BETAHISTINE DIHYDROCHLORIDE 16 mg

farmaceutische vorm:

TABLET

Samenstelling:

BETAHISTINE DIHYDROCHLORIDE 16 mg

Prescription-type:

POM

Therapeutisch gebied:

OTHER NERVOUS SYSTEM DRUGS

Autorisatie-status:

Withdrawn

Autorisatie datum:

2006-08-03

Bijsluiter

                                BETAHISTIN  ACTAVIS
Betahistine dihydrochloride, 8mg & 16mg tablets
PACKAGE LEAFLET: INFORMATION FOR THE USER
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU 
START TAKING THIS MEDICINE.
-  Keep this leaflet. You may need to read  
  it again.
-  If you have any further questions, ask  
  your doctor or pharmacist.
-  This medicine has been prescribed for  
  you. Do not pass it on to others. It may  
  harm them, even if their symptoms are  
  the same as yours.
-  If any of the side effects gets serious, or  
  if you notice any side effects not listed  
  in this leaflet, please tell your doctor or  
  pharmacist.
IN THIS LEAFLET: 
1.  What betahistine is and what it is used for
2.  Before you take betahistine
3.  How to take betahistine
4.  Possible side effects
5.  How to store betahistine
6.  Further information
 
 
1.  WHAT BETAHISTINE IS AND WHAT IT  
  IS USED FOR
Betahistine is a medicine that is used to treat 
symptoms of  Ménière’s syndrome such as 
dizziness, ringing in the ears, loss of hearing 
and nausea. 
2.  BEFORE YOU TAKE BETAHISTINE
DO NOT USE BETAHISTINE
•  if you are allergic (hypersensitive) to  
  betahistine or to any of the other  
  components of the tablet (see also  
  section 6 “Further information”)
•  if you have a phaeochromocytoma, a  
  rare tumour of the adrenal gland
•  if you are under the age of 18
•  if you are breast-feeding (see also the  
  section on “Pregnancy and breast- 
  feeding”).
 
TAKE SPECIAL CARE WITH BETAHISTINE
•  if you suffer or if you have suffered  
  from a stomach ulcer (peptic ulcer)
•  if you suffer from asthma
•  if you are suffering from nettle rash,  
  skin rash or a cold in the nose caused  
  by an allergy, since these complaints  
  may be exacerbated
•  if you have low blood pressure.
If you suffer from any of the above 
conditions, consult your doctor about 
whether you may take betahistine.
The above group
                                
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Productkenmerken

                                 
Page 1 of 5 
 
SUMMARY OF PRODUCT CHARACTERISTICS 
 
1. 
NAME OF THE MEDICINAL PRODUCT 
 
 
Betahistin Actavis 16mg Tablets 
 
 
2. 
QUALITATIVE AND QUANTITATIVE COMPOSITION 
 
 
One tablet contains 16 mg Betahistine dihydrochloride  
 
One tablet contains 140 mg lactose monohydrate. 
 
For a full list of excipients, see section 6.1 
 
 
3. 
PHARMACEUTICAL FORM 
 
 
Tablet. 
 
 
White or almost white round tablet. Embossed B16 on one side, scored reverse. 
 
The tablet can be divided into equal halves. 
 
 
4.  
CLINICAL PARTICULARS 
 
4.1 
THERAPEUTIC INDICATIONS 
 
 
Betahistine is indicated for the treatment of Ménière’s syndrome, symptoms of which 
may include vertigo, tinnitus, hearing loss and nausea   
 
4.2 
POSOLOGY AND METHOD OF ADMINISTRATION 
 
 
_Dosage _
 
 
Adults (including the elderly): 
 
Initial oral treatment is 8 to 16 mg three times daily, taken with food. 
 
Maintenance doses are generally in the range of 24 - 48 mg daily. Dosage can be 
adjusted to suit individual patient needs. Sometimes improvement can be observed 
after only a couple of weeks of treatment. 
 
 
 
Children and adolescents: 
 
Betahistine tablets are not recommended for use in children and adolescents below the 
age of 18 years due to lack of data on safety and efficacy.  
 
4.3 
CONTRAINDICATIONS 
 
 
Page 2 of 5 
 
Betahistine is contraindicated in patients with phaeochromocytoma. As betahistine is a 
synthetic analogue of histamine it may induce the release of catecholamines from the 
tumor resulting in severe hypertension. 
 
 
Also contraindicated in the cases of: 
•
 
hypersensitivity to the active substance or to any of the excipients. 
 
4.4 
SPECIAL WARNINGS AND PRECAUTIONS FOR USE 
 
 
Caution is advised in the
                                
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