Does SENNOSIDES Cause Product dose omission issue? 75 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Product dose omission issue have been filed in association with SENNOSIDES (Geri-kot). This represents 3.3% of all adverse event reports for SENNOSIDES.
75
Reports of Product dose omission issue with SENNOSIDES
3.3%
of all SENNOSIDES reports
9
Deaths
70
Hospitalizations
How Dangerous Is Product dose omission issue From SENNOSIDES?
Of the 75 reports, 9 (12.0%) resulted in death, 70 (93.3%) required hospitalization, and 9 (12.0%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SENNOSIDES. However, 75 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which SENNOSIDES Alternatives Have Lower Product dose omission issue Risk?
SENNOSIDES vs SENNOSIDES A AND B
SENNOSIDES vs SENSIPAR
SENNOSIDES vs SERETIDE
SENNOSIDES vs SEROQUEL
SENNOSIDES vs SERTRALINE