Does SENNOSIDES Cause Intentional product misuse? 306 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 306 reports of Intentional product misuse have been filed in association with SENNOSIDES (Geri-kot). This represents 13.4% of all adverse event reports for SENNOSIDES.
306
Reports of Intentional product misuse with SENNOSIDES
13.4%
of all SENNOSIDES reports
119
Deaths
14
Hospitalizations
How Dangerous Is Intentional product misuse From SENNOSIDES?
Of the 306 reports, 119 (38.9%) resulted in death, 14 (4.6%) required hospitalization, and 14 (4.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SENNOSIDES. However, 306 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which SENNOSIDES Alternatives Have Lower Intentional product misuse Risk?
SENNOSIDES vs SENNOSIDES A AND B
SENNOSIDES vs SENSIPAR
SENNOSIDES vs SERETIDE
SENNOSIDES vs SEROQUEL
SENNOSIDES vs SERTRALINE