Does PSYLLIUM HUSK Cause Condition aggravated? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Condition aggravated have been filed in association with PSYLLIUM HUSK (Quality Choice Fiber Laxative). This represents 8.7% of all adverse event reports for PSYLLIUM HUSK.
41
Reports of Condition aggravated with PSYLLIUM HUSK
8.7%
of all PSYLLIUM HUSK reports
36
Deaths
33
Hospitalizations
How Dangerous Is Condition aggravated From PSYLLIUM HUSK?
Of the 41 reports, 36 (87.8%) resulted in death, 33 (80.5%) required hospitalization, and 27 (65.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PSYLLIUM HUSK. However, 41 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which PSYLLIUM HUSK Alternatives Have Lower Condition aggravated Risk?
PSYLLIUM HUSK vs PULMICORT FLEXHALER
PSYLLIUM HUSK vs PYRAZINAMIDE
PSYLLIUM HUSK vs PYRIDOSTIGMINE
PSYLLIUM HUSK vs PYRIDOXINE
PSYLLIUM HUSK vs PYRIDOXINE\THIAMINE