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This would seem to support case studies reporting acrocyanosis as an unusual side effect for pediatric patients taking tricyclic antidepressants, as these medications can inhibit the reuptake of serotonin and thus increase their blood concentrations. [9] Acrocyanosis has been reported in association with many other medications and substances. [1]
It has also been used (in conjunction with sodium nitroprusside) successfully as an antidote to reverse the severe peripheral vasoconstriction which can occur as a result of overdose with certain 5-HT 2A agonist drugs such as 25I-NBOMe, [2] DOB and Bromodragonfly (prolonged severe vasoconstriction can lead to gangrene if untreated).
Type A: augmented pharmacological effects, which are dose-dependent and predictable [5]; Type A reactions, which constitute approximately 80% of adverse drug reactions, are usually a consequence of the drug's primary pharmacological effect (e.g., bleeding when using the anticoagulant warfarin) or a low therapeutic index of the drug (e.g., nausea from digoxin), and they are therefore predictable.
Two separate patients who were prescribed a popular class of antibiotic told WFTS the drug came with severe side effects. For both women, the family of antibiotics known as fluoroquinolones ...
Side effects may only last for a short time and then go away. Side effects can be relieved in some cases with non pharmacological treatment. [4] Some side effects require treatment to correct potentially serious and sometimes fatal reactions to penicillin. Penicillin has not been found to cause birth defects. [5]
Medication Antidepressants , anti-hypertension medication, or if caused by other reasons, naloxone hydrochloride Cyanosis is the change of body tissue color to a bluish-purple hue, as a result of decrease in the amount of oxygen bound to the hemoglobin in the red blood cells of the capillary bed . [ 1 ]
Hepatotoxicity, dermatological side effects, and abuse potential. [7] Aminopyrine: 1999 France, Thailand Risk of agranulocytosis and severe acne. [3] Amobarbital: 1980 Norway Risk of barbiturate toxicity. [3] Amoproxan: 1970 France Dermatologic and ophthalmic toxicity. [3] Anagestone acetate: 1969 Germany Animal carcinogenicity. [3] Antrafenine ...
Its use by mouth or by injection is only recommended when safer antibiotics cannot be used. [5] Monitoring both blood levels of the medication and blood cell levels every two days is recommended during treatment. [5] Common side effects include bone marrow suppression, nausea, and diarrhea. [5] The bone marrow suppression may result in death. [5]