Does PSYLLIUM HUSK Cause Product use issue? 160 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 160 reports of Product use issue have been filed in association with PSYLLIUM HUSK (Quality Choice Fiber Laxative). This represents 34.0% of all adverse event reports for PSYLLIUM HUSK.
160
Reports of Product use issue with PSYLLIUM HUSK
34.0%
of all PSYLLIUM HUSK reports
57
Deaths
5
Hospitalizations
How Dangerous Is Product use issue From PSYLLIUM HUSK?
Of the 160 reports, 57 (35.6%) resulted in death, 5 (3.1%) required hospitalization, and 3 (1.9%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PSYLLIUM HUSK. However, 160 reports have been filed with the FAERS database.
What Other Side Effects Does PSYLLIUM HUSK Cause?
Exposure during pregnancy (220)
Off label use (212)
Intentional product misuse (185)
Headache (173)
Hypertension (173)
Hyperhidrosis (171)
Food allergy (168)
Immunodeficiency (167)
Joint swelling (167)
Hepatic enzyme increased (166)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which PSYLLIUM HUSK Alternatives Have Lower Product use issue Risk?
PSYLLIUM HUSK vs PULMICORT FLEXHALER
PSYLLIUM HUSK vs PYRAZINAMIDE
PSYLLIUM HUSK vs PYRIDOSTIGMINE
PSYLLIUM HUSK vs PYRIDOXINE
PSYLLIUM HUSK vs PYRIDOXINE\THIAMINE