Does SENNOSIDES Cause Wrong product administered? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Wrong product administered have been filed in association with SENNOSIDES (Geri-kot). This represents 1.7% of all adverse event reports for SENNOSIDES.
39
Reports of Wrong product administered with SENNOSIDES
1.7%
of all SENNOSIDES reports
17
Deaths
22
Hospitalizations
How Dangerous Is Wrong product administered From SENNOSIDES?
Of the 39 reports, 17 (43.6%) resulted in death, 22 (56.4%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SENNOSIDES. However, 39 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which SENNOSIDES Alternatives Have Lower Wrong product administered Risk?
SENNOSIDES vs SENNOSIDES A AND B
SENNOSIDES vs SENSIPAR
SENNOSIDES vs SERETIDE
SENNOSIDES vs SEROQUEL
SENNOSIDES vs SERTRALINE