Does ACYCLOVIR Cause Intentional product use issue? 138 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 138 reports of Intentional product use issue have been filed in association with ACYCLOVIR (Acyclovir). This represents 1.0% of all adverse event reports for ACYCLOVIR.
138
Reports of Intentional product use issue with ACYCLOVIR
1.0%
of all ACYCLOVIR reports
52
Deaths
69
Hospitalizations
How Dangerous Is Intentional product use issue From ACYCLOVIR?
Of the 138 reports, 52 (37.7%) resulted in death, 69 (50.0%) required hospitalization, and 19 (13.8%) 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 ACYCLOVIR. However, 138 reports have been filed with the FAERS database.
What Other Side Effects Does ACYCLOVIR Cause?
Drug ineffective (1,727)
Acute kidney injury (1,405)
Off label use (942)
Headache (694)
Condition aggravated (584)
Pyrexia (565)
Nausea (537)
Rash (461)
Neurotoxicity (460)
Dyspnoea (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 ACYCLOVIR Alternatives Have Lower Intentional product use issue Risk?
ACYCLOVIR vs AD26.COV2.S
ACYCLOVIR vs ADAGRASIB
ACYCLOVIR vs ADALIMUMAB
ACYCLOVIR vs ADALIMUMAB-AACF
ACYCLOVIR vs ADALIMUMAB-AATY