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Drug-induced liver injury (DILI) is a cause of acute and chronic liver disease caused specifically by medications and the most common reason for a drug to be withdrawn from the market after approval. The liver plays a central role in transforming and clearing chemicals and is susceptible to the toxicity from these agents.
Myelosupression, embryo-fetal toxicity, hepatotoxicity (rare) [19] Trabectedin: IV Alkylates DNA. Advanced liposarcoma and leimyosarcoma Bone marrow suppression, rhabdomyolysis, embryo-fetal toxicity, capillary leak syndrome, hepatotoxicity [20] 1.10 Platinum compounds: Carboplatin: IV: Reacts with DNA, inducing apoptosis, non-cell cycle specific.
The symptoms can often be divided into differing toxidromes. This can help one determine what class of drug or toxin is causing the difficulties. Symptoms of opioid overdoses include slow breathing, heart rate and pulse. [6] Opioid overdoses can also cause pinpoint pupils, and blue lips and nails due to low levels of oxygen in the blood.
Hepatotoxicity. [3] Dimazole (Diamthazole) 1972 France, US Neuropsychiatric reaction. [3] Dimethylamylamine (DMAA) 1983 US Voluntarily withdrawn from market by Lily. [17]: 12 Reintroduced as a dietary supplement in 2006; [17]: 13 in 2013 the FDA started work to ban it due to cardiovascular problems [18] Dinoprostone: 1990 UK
Sevoflurane has an excellent safety record, [13] but is under review for potential hepatotoxicity, and may accelerate Alzheimer's. [16] There were rare reports involving adults with symptoms similar to halothane hepatotoxicity. [13] Sevoflurane is the preferred agent for mask induction due to its lesser irritation to mucous membranes.
You already know that drinking alcohol can wreak havoc on your liver. (And if you don't, well, here are more details on those dangers.) ... (Epigallocatechin-3-gallate, one of the catechins in ...
Drug-drug interactions can be of serious concern for patients who are undergoing multi-drug therapies. [5] Coadministration of chloroquine , an anti-malaria drug, and statins for treatment of cardiovascular diseases has been shown to cause inhibition of organic anion-transporting polypeptides (OATPs) and lead to systemic statin exposure.
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