Betahistine Dihydrochloride Tablets 8mg
Betahistine Dihydrochloride Tablets 8mg
Each tablet contains Betahistine dihydrochloride 8 mg Excipient(s) with known effect: Each tablet contains 50 mg lactose For a full list of excipients, see section 6.1.
Tablets for oral administration
Flat white tablets, with bevelled edge. Markings: R3 on one side scoreline on the reverse.
The score line is only to facilitate breaking for ease of swallowing and not to divide into equal doses.
Betahistine is indicated for the treatment of vertigo, tinnitus and hearing loss associated with Meniere’s syndrome.
Adults (including the elderly);
Initially 16mg 3 times daily, taken preferably with meals.
Maintenance doses are generally in the range 24-48mg daily.
Paediatric population: not recommended for use in children below 18 years due to insufficient data on safety and efficacy.
Geriatric population: although there are limited data from clinical studies in this patient group, extensive post marketing experience suggests that no dose adjustment
Renal impairment: there are no specific clinical trials available in this patient group, but according to post-marketing experience no dose adjustment appears to be necessary.
Hepatic impairment: there are no specific clinical trials available in this patient group, but according to post-marketing experience no dose adjustment appears to be necessary.
Method of Administration:
Swallow the tablet with water.
Betahistine is contraindicated in patients with a phaeochromocytoma and hypersensitivity to betahistine dihydrochloride or any of the excipients listed in section 6.1.
Caution is advised in the treatment of patients with a history of peptic ulcer. Clinical intolerance to betahistine dihydrochloride in bronchial asthma patients has been shown in a relatively few patients and therefore caution should be exercised when administering betahistine to patients with bronchial asthma.
Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.
No in-vivo interaction studies have been performed. Based on in-vitro data no in-vivo inhibition on Cytochrome P450 enzymes is expected.
In vitro data indicate an inhibition of betahistine metabolism by drugs that inhibit monoamino-oxidase (MAO) including MAO subtype B (e.g. selegiline). Caution is recommended when using betahistine and MAO inhibitors (including MAO-B selective) concomitantly.
As betahistine is an analogue of histamine, interaction of betahistine with antihistamines may in theory affect the efficacy of one of these drugs.
There are no adequate data from the use of betahistine in pregnant women. Animal studies are insufficient with respect to effects on pregnancy, embryonal/foetal development, parturition and postnatal development. The potential risk for humans is unknown. Betahistine should not be used during pregnancy unless clearly necessary.
It is not known whether betahistine is excreted in human milk. There are no animal studies on the excretion of betahistine in milk. The importance of the drug to the mother should be weighed against the benefits of nursing and the potential risks for the child.
Vertigo, tinnitus and hearing loss associated with Meniere’s syndrome can negatively affect the ability to drive and use machines. In clinical studies specifically designed to investigate the ability to drive and use machines betahistine had no or negligible effects.
The following undesirable effects have been experienced with the below indicated frequencies in betahistine-treated patients in placebo-controlled clinical trials [very common (>1/10); common (>1/100 to <1/10); uncommon (>1/1,000 to<1/100); rare (>1/10,000 to <1/1,000); very rare (<1/10,000)].
Common: nausea and dyspepsia
Nervous System disorders:
In addition to those events reported during clinical trials, the following undesirable effects have been reported spontaneously during post-marketing use and in scientific literature. A frequency cannot be estimated from the available data and is therefore classified as “not known”.
Immune System disorders:
Hypersensitivity reactions, e.g. anaphylaxis have been reported.
Mild gastric complaints (e.g. vomiting, gastrointestinal pain, abdominal distension and bloating) have been observed. These can normally be dealt with by taking the dose during meals or by lowering the dose.
Skin and subcutaneous tissue disorders:
Cutaneous and subcutaneous hypersensitivity reactions have been reported, in particular angioneurotic oedema, urticaria, rash, and pruritus.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions
via the national reporting system via Yellow Card Scheme at www.mhra.gov .uk/yellowcard.
A few overdose cases have been reported. Some patients experienced mild to moderate symptoms with doses up to 640 mg (e.g. nausea, somnolence, abdominal pain). More serious complications (e.g. convulsion, pulmonary or cardiac complications) were observed in cases of intentional overdose of betahistine especially in combination with other overdosed drugs. Treatment of overdose should include standard supportive measures
Pharmacotherapeutic group :Antivertigo preparation. ATC Code: NO7CA01
The mechanism of action of betahistine is only partly understood. There are several plausible hypotheses that are supported by animal studies and human data:
• Betahistine affects the histaminergic system:
Betahistine acts both as a partial histamine H1-receptor agonist and histamine H3-receptor antagonist also in neuronal tissue, and has negligible H2-receptor activity. Betahistine increases histamine turnover and release by blocking presynaptic H3-receptors and inducing H3-receptor downregulation.
• Betahistine may increase blood flow to the cochlear region as well as to the whole brain:
Pharmacological testing in animals has shown that the blood circulation in the striae vascularis of the inner ear improves, probably by means of a relaxation of the precapillary sphincters of the microcirculation of the inner ear. Betahistine was also shown to increase cerebral blood flow in humans.
• Betahistine facilitates vestibular compensation:
Betahistine accelerates the vestibular recovery after unilateral neurectomy in animals, by promoting and facilitating central vestibular compensation; this effect characterized by an up-regulation of histamine turnover and release, is mediated via the H3 Receptor antagonism. In human subjects, recovery time after vestibular neurectomy was also reduced when treated with betahistine.
• Betahistine alters neuronal firing in the vestibular nuclei:
Betahistine was also found to have a dose dependent inhibiting effect on spike generation of neurons in lateral and medial vestibular nuclei.
The pharmacodynamic properties as demonstrated in animals may contribute to the therapeutic benefit of betahistine in the vestibular system.
The efficacy of betahistine was shown in studies in patients with vestibular vertigo and with Meniere’s disease as was demonstrated by improvements in severity and frequency of vertigo attacks
Orally administered betahistine is readily and almost completely absorbed from all parts of the gastro-intestinal tract. After absorption, the drug is rapidly and almost completely metabolized into 2-pyridylacetic acid. Plasma levels of betahistine are very low. Pharmacokinetic analyses are therefore based on 2-PAA measurements in plasma and urine.
Under fed conditions Cmax is lower compared to fasted conditions. However, total absorption of betahistine is similar under both conditions, indicating that food intake only slows down the absorption of betahistine.
The percentage of betahistine that is bound by blood plasma proteins is less than 5 %.
After absorption, betahistine is rapidly and almost completely metabolized into 2-PAA (which has no pharmacological activity).
After oral administration of betahistine the plasma (and urinary) concentration of 2-PAA reaches its maximum 1 hour after intake and declines with a halflife of about 3.5 hours.
2-PAA is readily excreted in the urine. In the dose range between 8 and 48 mg, about 85% of the original dose is recovered in the urine. Renal or faecal excretion of betahistine itself is of minor importance.
Recovery rates are constant over the oral dose range of 8 - 48 mg indicating that the pharmacokinetics of betahistine are linear, and suggesting that the involved metabolic pathway is not saturated.
Repeat oral dose toxicity studies in dogs and rats for 6 and 18 months respectively revealed no clinically relevant adverse effects. Betahistine was not mutagenic in conventional in vitro and in vivo studies of genotoxicity. Histopathological examination in the 18 months chronic toxicity study indicated no carcinogenic effects. However, specific carcinogenicity studies were not performed with
Betahistine. Limited studies of reproductive toxicity in rats and rabbits showed no teratogenic effects.
Lactose Citric acid
Microcrystalline cellulose Maize starch Crospovidone Povidone K25 Sodium stearyl fumarate
There are no major incompatibilities.
A shelf-life of 24 months is recommended for Betahistine dihydrochloride tablets.
Store below 30°C.
Betahistine Dihydrochloride 8mg Tablets are packed in blister packs contained in a cardboard carton.
Pack sizes: 84, 100 and 120 Tablets
Not all pack sizes may be marketed.
RI Pharma Ltd,
First Floor, 6 St. John's Court,
Upper Fforest Way,
Swansea Enterprise Park,
Wales SA6 8QQ