Does PSYLLIUM HUSK Cause Intentional product misuse? 185 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 185 reports of Intentional product misuse have been filed in association with PSYLLIUM HUSK (Quality Choice Fiber Laxative). This represents 39.4% of all adverse event reports for PSYLLIUM HUSK.
185
Reports of Intentional product misuse with PSYLLIUM HUSK
39.4%
of all PSYLLIUM HUSK reports
87
Deaths
31
Hospitalizations
How Dangerous Is Intentional product misuse From PSYLLIUM HUSK?
Of the 185 reports, 87 (47.0%) resulted in death, 31 (16.8%) required hospitalization, and 30 (16.2%) 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 PSYLLIUM HUSK. However, 185 reports have been filed with the FAERS database.
What Other Side Effects Does PSYLLIUM HUSK Cause?
Exposure during pregnancy (220)
Off label use (212)
Headache (173)
Hypertension (173)
Hyperhidrosis (171)
Food allergy (168)
Immunodeficiency (167)
Joint swelling (167)
Hepatic enzyme increased (166)
Hypersensitivity (165)
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 PSYLLIUM HUSK Alternatives Have Lower Intentional product misuse Risk?
PSYLLIUM HUSK vs PULMICORT FLEXHALER
PSYLLIUM HUSK vs PYRAZINAMIDE
PSYLLIUM HUSK vs PYRIDOSTIGMINE
PSYLLIUM HUSK vs PYRIDOXINE
PSYLLIUM HUSK vs PYRIDOXINE\THIAMINE