A more recent double-blind trial compared the combination to betahistine in 306 patients with peripheral vestibular vertigo. Approximately 55% of the patients had a Ménière-like symptom complex, but patients with confirmed Ménière’s disease were excluded. A 12-item scale was used to calculate a mean vertigo score. After four weeks this composite score had declined by 67.5% in the patients taking the combination and by 59.5% in those taking betahistine. Approximately 71% of the 152 patients randomised to the combination felt much improved or very much improved compared with 63% of the betahistine group.2
In the analysis of five trials, the most frequent adverse effects seen with the combination of cinnarizine and dimenhydrinate were fatigue, somnolence, dry mouth, headache and abdominal pain. The sedative effects may be increased by other drugs, including alcohol, which depress the central nervous system. As the combination has some anticholinergic effects, it is contraindicated in patients with angle-closure glaucoma or urinary retention. Convulsions, raised intracranial pressure and alcohol abuse are also contraindications. Cinnarizine has been associated with extrapyramidal effects including tardive dyskinesia. As these effects may be irreversible, the combination should only be used for short-term management.
Combining cinnarizine with dimenhydrinate has a greater effect on vertigo than either drug alone, but the difference may be small. For example, in the five-trial analysis there was a difference of approximately two points between the combination and cinnarizine 20 mg on the 40-point vertigo score (see Table).1 However, cinnarizine is not available on its own in Australia. Although there is European experience with the combination, it is only indicated in Australia for adults who have not responded to other treatments. In view of the uncertainty about long-term safety, treatment should not usually exceed four weeks.
🅃 manufacturer provided the product information
The Transparency Score is explained in New drugs: transparency, Vol 37 No 1, Aust Prescr 2014;37:27.
At the time the comment was prepared, information about this drug was available on the websites of the Food and Drug Administration in the USA, the European Medicines Agency and the Therapeutic Goods Administration.