Does DESVENLAFAXINE Cause Intentional product use issue? 88 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 88 reports of Intentional product use issue have been filed in association with DESVENLAFAXINE (Desvenlafaxine Succinate). This represents 1.0% of all adverse event reports for DESVENLAFAXINE.
88
Reports of Intentional product use issue with DESVENLAFAXINE
1.0%
of all DESVENLAFAXINE reports
0
Deaths
12
Hospitalizations
How Dangerous Is Intentional product use issue From DESVENLAFAXINE?
Of the 88 reports, 12 (13.6%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESVENLAFAXINE. However, 88 reports have been filed with the FAERS database.
What Other Side Effects Does DESVENLAFAXINE Cause?
Drug ineffective (1,576)
Anxiety (679)
Feeling abnormal (671)
Dizziness (605)
Nausea (575)
Headache (548)
Depression (542)
Withdrawal syndrome (530)
Malaise (512)
Insomnia (428)
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 DESVENLAFAXINE Alternatives Have Lower Intentional product use issue Risk?
DESVENLAFAXINE vs DETROL
DESVENLAFAXINE vs DEUCRAVACITINIB
DESVENLAFAXINE vs DEUTETRABENAZINE
DESVENLAFAXINE vs DEUTIVACAFTOR\TEZACAFTOR\VANZACAFTOR
DESVENLAFAXINE vs DEVICE