Does DESVENLAFAXINE Cause Condition aggravated? 288 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 288 reports of Condition aggravated have been filed in association with DESVENLAFAXINE (Desvenlafaxine Succinate). This represents 3.2% of all adverse event reports for DESVENLAFAXINE.
288
Reports of Condition aggravated with DESVENLAFAXINE
3.2%
of all DESVENLAFAXINE reports
2
Deaths
43
Hospitalizations
How Dangerous Is Condition aggravated From DESVENLAFAXINE?
Of the 288 reports, 2 (0.7%) resulted in death, 43 (14.9%) required hospitalization, and 6 (2.1%) 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 DESVENLAFAXINE. However, 288 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 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 DESVENLAFAXINE Alternatives Have Lower Condition aggravated Risk?
DESVENLAFAXINE vs DETROL
DESVENLAFAXINE vs DEUCRAVACITINIB
DESVENLAFAXINE vs DEUTETRABENAZINE
DESVENLAFAXINE vs DEUTIVACAFTOR\TEZACAFTOR\VANZACAFTOR
DESVENLAFAXINE vs DEVICE