Does SENNOSIDES Cause Intentional product use issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with SENNOSIDES (Geri-kot). This represents 0.9% of all adverse event reports for SENNOSIDES.
21
Reports of Intentional product use issue with SENNOSIDES
0.9%
of all SENNOSIDES reports
3
Deaths
8
Hospitalizations
How Dangerous Is Intentional product use issue From SENNOSIDES?
Of the 21 reports, 3 (14.3%) resulted in death, 8 (38.1%) required hospitalization, and 4 (19.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SENNOSIDES. However, 21 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which SENNOSIDES Alternatives Have Lower Intentional product use issue Risk?
SENNOSIDES vs SENNOSIDES A AND B
SENNOSIDES vs SENSIPAR
SENNOSIDES vs SERETIDE
SENNOSIDES vs SEROQUEL
SENNOSIDES vs SERTRALINE