Does SENNOSIDES Cause Product use issue? 324 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 324 reports of Product use issue have been filed in association with SENNOSIDES (Geri-kot). This represents 14.2% of all adverse event reports for SENNOSIDES.
324
Reports of Product use issue with SENNOSIDES
14.2%
of all SENNOSIDES reports
108
Deaths
6
Hospitalizations
How Dangerous Is Product use issue From SENNOSIDES?
Of the 324 reports, 108 (33.3%) resulted in death, 6 (1.9%) required hospitalization, and 7 (2.2%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SENNOSIDES. However, 324 reports have been filed with the FAERS database.
What Other Side Effects Does SENNOSIDES Cause?
Asthma (706)
Fatigue (636)
Pain (584)
Hyperhidrosis (575)
Headache (560)
Constipation (549)
Upper respiratory tract infection (529)
Fluid retention (511)
Pyrexia (457)
Drug hypersensitivity (433)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which SENNOSIDES Alternatives Have Lower Product use issue Risk?
SENNOSIDES vs SENNOSIDES A AND B
SENNOSIDES vs SENSIPAR
SENNOSIDES vs SERETIDE
SENNOSIDES vs SEROQUEL
SENNOSIDES vs SERTRALINE