Abstract
Recently, the European Medicines Agency (EMEA) and the Committee on Herbal Medicinal Products (HMPC) have released a public statement to draw the attention of European health authorities to 42 cases (34 directly reported from European national competent authorities and 8 published) of suspected hepatotoxic reactions to Cimicifugae racemosae rhizoma (black cohosh, root) in patients, probably all of them women, who were treated for menopause-related disorders. Following a review of all data available, this statement assumes a connection between herbal medicinal products that contain Cimicifugae racemosae rhizoma and human hepatotoxic adverse reactions. Nevertheless, this highly authoritative review of such an impressive number of cases concludes in its summary that ‘Overall, all discussed cases of literature and pharmacovigilance reports are poorly documented,’ and only ‘two can be considered as possible’ and ‘two can be classified as probable’ [1, p 9]: (1) In case 28, according to the numeration in the EMEA statement, RUCAM score 4, the only case directly collected from European national competent authorities, the adverse reaction was considered possible, but information on differential diagnostic assessment was not available. The patient consumed 80 mg of an unknown extract daily and for an unknown period. (2) In another case report [2] (RUCAM score 3) the patient was a 54-year-old woman suffering from hypothyroidism, fibromyalgia, osteoarthritis and depression. She had taken 1,000 mg black cohosh (unclear, if a type of extract or crude drug) daily for several months. The patient was on fluoxetine, propoxyphene and paracetamol (a well known hepatotoxic substance) concomitantly and used to drink 2 glasses of wine in the evenings. The statement claims ‘that since there is no further information on the herbal preparation, the case report is not of great relevance in the assessment of cimicifuga-related hepatotoxicity’ [1]. (3) A 57-year-old multimorbid Afro-American woman [3] (RUCAM score 7) with a history of polymyositis had developed an autoimmune hepatitis about 3 weeks after the first intake of Cimicifugae racemosae rhizoma (brand and dose unknown; no information if it was a combination product). After discontinuation of Cimicifugae racemosae rhizoma intake and starting a therapy with steroids and azathioprine, the patient recovered. Here, autoimmune hepatitis may as well have been a manifestation of a multisystem autoimmune disease. According to the draft recommendations of the Scientific Advisory Panel Subgroups on Hepatotoxicity, the case could be classified as idiosyncratic liver necrosis. Inititally, the causal relationship to black cohosh in this case was assessed ‘unclassifiable’, as information concerning the reaction was considered incomplete and inconsistent, and the follow-up publication includes more (although to some extent still inconsistent) information about the therapy [1]). (4) In another well-documented case [4] (RUCAM score 6) the dose administered was 500 mg/day. The reaction was described as hepatocellular, other causes of acute hepatitis were excluded. The provisional clinical diagnosis was autoimmune hepatitis. Therapy started with 60 mg prednisone / day for 5 weeks. Liver enzymes improved, but due to an aggravation of coagulopathy and encephalopathy, the patient underwent orthotopic liver transplantation. In the explanted organ, histological features of acute hepatitis, fibrous linkage of portal tracts and cholestasis were observed after 5 weeks on corticosteroids. Yet, in this case, too, the exact content of the remedy based on black cohosh is unclear, and it is not reported if it was an extract or crude drug, and if it contained other toxic substances, i.e. heavy metals. Later, Levitsky [4] reported that the patient neither drank, nor used drugs, nor took any other medication. However, in a US District Court proceeding the woman admitted that she regularly consumed alcohol, and used large doses of ibuprofen, a non-steroidal anti-inflamma-
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