N/A
Manufactured by ACTAVIS PHARMA, INC.
5 FDA adverse event reports analyzed
Last updated: 2026-04-15
BAPTISIA TINCTORIA ROOT is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by ACTAVIS PHARMA, INC.. The most commonly reported adverse reactions for BAPTISIA TINCTORIA ROOT include HOT FLUSH, LYMPHADENOPATHY, PARAESTHESIA ORAL, PRURITUS, URTICARIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for BAPTISIA TINCTORIA ROOT.
Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.
This profile reflects 5 FDA FAERS reports that mention BAPTISIA TINCTORIA ROOT. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include HOT FLUSH, LYMPHADENOPATHY, PARAESTHESIA ORAL, PRURITUS, URTICARIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list ACTAVIS PHARMA, INC. in connection with BAPTISIA TINCTORIA ROOT. Always verify the specific product and NDC with your pharmacist.