Does GLUTATHIONE Cause Condition aggravated? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Condition aggravated have been filed in association with GLUTATHIONE (Dark Spot Corrector Serum). This represents 17.5% of all adverse event reports for GLUTATHIONE.
26
Reports of Condition aggravated with GLUTATHIONE
17.5%
of all GLUTATHIONE reports
4
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From GLUTATHIONE?
Of the 26 reports, 4 (15.4%) resulted in death, 7 (26.9%) required hospitalization, and 3 (11.5%) 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 GLUTATHIONE. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does GLUTATHIONE Cause?
Dyspnoea (24)
Pain (22)
Drug ineffective (20)
Chest pain (19)
Malaise (19)
Cough (17)
Seizure (17)
Stomatitis (17)
Eczema (16)
Eosinophil count increased (16)
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 GLUTATHIONE Alternatives Have Lower Condition aggravated Risk?
GLUTATHIONE vs GLYBURIDE
GLUTATHIONE vs GLYBURIDE\METFORMIN
GLUTATHIONE vs GLYCERIN
GLUTATHIONE vs GLYCERIN\SORBITOL
GLUTATHIONE vs GLYCEROL PHENYLBUTYRATE