Does DESVENLAFAXINE Cause Product prescribing error? 62 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Product prescribing error have been filed in association with DESVENLAFAXINE (Desvenlafaxine Succinate). This represents 0.7% of all adverse event reports for DESVENLAFAXINE.
62
Reports of Product prescribing error with DESVENLAFAXINE
0.7%
of all DESVENLAFAXINE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Product prescribing error From DESVENLAFAXINE?
Of the 62 reports, 11 (17.7%) required hospitalization, and 2 (3.2%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESVENLAFAXINE. However, 62 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which DESVENLAFAXINE Alternatives Have Lower Product prescribing error Risk?
DESVENLAFAXINE vs DETROL
DESVENLAFAXINE vs DEUCRAVACITINIB
DESVENLAFAXINE vs DEUTETRABENAZINE
DESVENLAFAXINE vs DEUTIVACAFTOR\TEZACAFTOR\VANZACAFTOR
DESVENLAFAXINE vs DEVICE