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Showing posts with label Nimesulide. Show all posts
Showing posts with label Nimesulide. Show all posts

Friday, March 13, 2009

A case report on nimesulide and its relation with angina

Salman, M. T.; Rahman, S. Z. and Khan, R. A. (2003) A case report on nimesulide and its relation with angina. In: International Workshop on Adverse Drug-Reaction Monitoring & 3rd Annual Conference Society of Pharmacovigilance, India, 11-13 Dec 2003, Agra, India.

Even though there might be several cases of NSAIDs induced angina that are not been reported, we could find a definite case of Nimesulide induced angina in Aligarh. A 65 year old female patient was a known case of diabetes mellitis for 17 years and angina pectoris for 10 years for which she was maintained on drugs. She sustained injury after falling down and was found to have Colle’s fracture for which she was advised POP and Tab Nimesulide twice daily alongwith ongoing treatment. On 3rd day, she felt chest pain (angina) for which she used Tab sorbitrate 3-4 times a day but no improvement was noticed. Then she consulted her family physician. On examination, no abnormality was found except that ECG showed changes of ischemia and extra systoles. She was diagnosed as a case of Unstable Angina and advised to stop the suspected drug Nimesulide but continue to take previous treatment. She then showed improvement in angina. As an alternative Tab Brufen (Ibuprofen) 400 mg thrice daily was advised. The patient afterwards complained no problem. In this case, the unstable angina appears to be due to coronary spasm and not due to clot because on withdrawing the suspected drug there was rapid relief. The spasm seems to be related to inherent properties of Nimesulide and not due to prostaglandin inhibition as Brufen did not cause the same symptoms. Alternatively, it may be due to an imbalance between COX 1 and COX 2 activities due to preferencial COX 2 inhibition. Moreover, the inhibition of prostaglandin synthesis may adversely affect cardiovascular homeostasis.

Thursday, March 12, 2009

Serious hepatic reactions associated with the dietary supplement Fortodol

Herb-based dietary supplement contained active drug substance.
> The Medical Products Agency issues a warning against the herb-based dietary supplement Fortodol. The product has been on sale in Sweden since 2004. Analyses of the product revealed that it contains the drug substance nimesulide which is suspected to have caused serious liver injuries including liver failure and cardiovascular events with fatal outcome. At least 240 000 jars totalling 24 million capsules is reported having been sold in Sweden and Norway since 2004.
> The Medical Products Agency has received information about four cases of liver damage among Swedish patients who have taken Fortodol. In one of the cases, this led to acute liver failure resulting in death of the patient. The Norwegian Medical Products Agency has information about five cases of liver damage, and one case of death, with temporal association with the intake of Fortodol. It is known that the substance nimesulide can cause serious liver injury. Nimesulide is not an approved medicinal product in Sweden.
>  People consuming Fortodol should immediately cease the intake of it. Should you suffer from symptoms such as poor appetite, nausea, vomiting, abdominal pain, fatigue, dark urine or yellow skin, you should contact a medical care facility for a liver check up, says Barbro Gerdén, physician at the Medical Products Agency.
> The dietary supplement Fortodol, which is on sale on the Internet and in health food shops is said to relieve arthritis and muscle pains as well as head aches. The table of contents specifies that the product contains turmeric extract and the amino acid dl-phenylalanine. In two of nine analysed batches, the Medical Products Agency found the drug substance nimesulide.
> In those EU-countries where nimesulide is approved as a medicinal product the recommendations state that the substance should only be used for temporary treatments with prescriptions of not more than 30 doses. Fortodol has been sold in packages of up to 100 capsules.
> This is a product which has been launched as a dietary supplement, not as a medicinal product which implies a risk that people use it for longer periods of time, says Per Claeson, pharmacist at the Medical Products Agency.
> This is not the first time that the Medical Products Agency finds hazardous levels of drug substances in products sold as herbal products. Earlier examples are weight loss products and potency enhancers. This is the first time that an illegal drug substance has been discovered in a product used by people with painful disease states such as joint and muscle ailments. 

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