Does TRANYLCYPROMINE Cause Condition aggravated? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Condition aggravated have been filed in association with TRANYLCYPROMINE (Tranylcypromine). This represents 4.2% of all adverse event reports for TRANYLCYPROMINE.
16
Reports of Condition aggravated with TRANYLCYPROMINE
4.2%
of all TRANYLCYPROMINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Condition aggravated From TRANYLCYPROMINE?
Of the 16 reports, 5 (31.3%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRANYLCYPROMINE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does TRANYLCYPROMINE Cause?
Hypertensive crisis (53)
Contraindicated product administered (50)
Drug interaction (44)
Depression (41)
Hypertension (39)
Headache (33)
Drug ineffective (30)
Insomnia (30)
Serotonin syndrome (30)
Dizziness (27)
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 TRANYLCYPROMINE Alternatives Have Lower Condition aggravated Risk?
TRANYLCYPROMINE vs TRASTUZUMAB
TRANYLCYPROMINE vs TRASTUZUMAB-ANNS
TRANYLCYPROMINE vs TRASTUZUMAB DERUXTECAN
TRANYLCYPROMINE vs TRASTUZUMAB-DKST
TRANYLCYPROMINE vs TRASTUZUMAB-DTTB