Does ALPHA.-TOCOPHEROL, D- Cause Condition aggravated? 94 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Condition aggravated have been filed in association with ALPHA.-TOCOPHEROL, D- (Multi-Vit-Flor). This represents 16.0% of all adverse event reports for ALPHA.-TOCOPHEROL, D-.
94
Reports of Condition aggravated with ALPHA.-TOCOPHEROL, D-
16.0%
of all ALPHA.-TOCOPHEROL, D- reports
44
Deaths
54
Hospitalizations
How Dangerous Is Condition aggravated From ALPHA.-TOCOPHEROL, D-?
Of the 94 reports, 44 (46.8%) resulted in death, 54 (57.4%) required hospitalization, and 56 (59.6%) 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 ALPHA.-TOCOPHEROL, D-. However, 94 reports have been filed with the FAERS database.
What Other Side Effects Does ALPHA.-TOCOPHEROL, D- Cause?
Drug ineffective (321)
Macular degeneration (270)
Off label use (204)
Therapeutic product effect incomplete (194)
Nausea (155)
Weight decreased (136)
Pain (133)
Malaise (131)
Pyrexia (131)
Chronic sinusitis (129)
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 ALPHA.-TOCOPHEROL, D- Alternatives Have Lower Condition aggravated Risk?
ALPHA.-TOCOPHEROL, D- vs ALPHA.-TOCOPHEROL, DL-
ALPHA.-TOCOPHEROL, D- vs ALPHA.1-PROTEINASE INHIBITOR HUMAN
ALPHA.-TOCOPHEROL, D- vs ALPRAZOLAM
ALPHA.-TOCOPHEROL, D- vs ALPROSTADIL
ALPHA.-TOCOPHEROL, D- vs ALTEPLASE