The most commonly reported side effects of tubocurarine include drug interaction, drug dependence, and hypertension, based on 18 FDA adverse event reports from 2004 to 2023.
Percentages show how often each reaction appears relative to total reports for tubocurarine.
These are voluntary reports and do not establish that tubocurarine caused these reactions.
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Other drugs that appear in adverse event reports alongside tubocurarine. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
38.9% of tubocurarine adverse event reports involve female patients and 38.9% involve male patients. The largest age group is adult at 83%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking tubocurarine when the adverse event was reported.
Tubocurarine is sold under the brand name Tubocurarine Chloride.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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