Buproban was first marketed in Australia late in 2000 as a short-term aid to giving up smoking and has had very high usage. It was initially developed as an antidepressant. It is a selective inhibitor of the neuronal re-uptake of catecholamines in the brain but its mechanism to enhance the ability to quit smoking is unknown. New medicines achieve registration on the basis of experience in relatively limited numbers of patients and some uncommon or rare adverse reactions to the drug become recognised only after usage has grown, which may take years. In contrast, the very high usage of Buproban in a short time has highlighted several possible adverse effects, some of which may be severe.
Other names for this medication:
Bupropion,
Amfebutamone,
Aplenzin,
Buproban,
Bupropiona,
Buxon,
Dosier,
Quomem,
Wellbutrin,
Zyntabac,
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Ranitic,
Emilok,
Clabel,
Cipamox,
Cimal,
Citoles,
Capro,
Repligen,
Medocycline,
Letonal,
Rhinolast,
Depramine,
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Detection of an involvement of the human mismatch repair genes hMLH1 and hMSH2 in nucleotide excision repair tropargal y glaucoma symptoms is dependent on UVC fluence to cells. The authors have analysed cases of this rare form of post-traumatic pathology referred in the literature since 1941, examining them from a clinical, therapeutic and prognostic point of view. Geographic distribution of the population and management of natural resources in the Sahel Incorporation of radiolabelled amino acids by adult Schistosoma japonicum: further characterization of a putative eggshell precursor protein. The sartorius muscle transposition in the treatment of deep wound infection after vascular surgery in the groin.
A patient in her 60s with systemic lupus erythematosus presented to an outpatient dermatology clinic on multiple occasions, with exacerbations of cutaneous lupus after exposure to surgical lighting during vyfat medicine cabinets dental procedures. However, the mutant was still able to grow and divide at low growth rates with doubling times similar to those for the wild-type strain, indicating that trehalose and glycogen are not essential for cell cycle progression.
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