Does TOZINAMERAN Cause Intentional product use issue? 149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 149 reports of Intentional product use issue have been filed in association with TOZINAMERAN. This represents 2.2% of all adverse event reports for TOZINAMERAN.
149
Reports of Intentional product use issue with TOZINAMERAN
2.2%
of all TOZINAMERAN reports
3
Deaths
23
Hospitalizations
How Dangerous Is Intentional product use issue From TOZINAMERAN?
Of the 149 reports, 3 (2.0%) resulted in death, 23 (15.4%) required hospitalization, and 3 (2.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOZINAMERAN. However, 149 reports have been filed with the FAERS database.
What Other Side Effects Does TOZINAMERAN Cause?
Fatigue (1,197)
Headache (904)
Covid-19 (896)
Pain in extremity (675)
Pyrexia (665)
Pain (633)
Drug ineffective (547)
Nausea (473)
Arthralgia (464)
Off label use (446)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which TOZINAMERAN Alternatives Have Lower Intentional product use issue Risk?
TOZINAMERAN vs TRABECTEDIN
TOZINAMERAN vs TRACLEER
TOZINAMERAN vs TRADJENTA
TOZINAMERAN vs TRALOKINUMAB-LDRM
TOZINAMERAN vs TRAMADOL