Does TREPROSTINIL DIOLAMINE Cause Condition aggravated? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Condition aggravated have been filed in association with TREPROSTINIL DIOLAMINE. This represents 6.8% of all adverse event reports for TREPROSTINIL DIOLAMINE.
17
Reports of Condition aggravated with TREPROSTINIL DIOLAMINE
6.8%
of all TREPROSTINIL DIOLAMINE reports
4
Deaths
15
Hospitalizations
How Dangerous Is Condition aggravated From TREPROSTINIL DIOLAMINE?
Of the 17 reports, 4 (23.5%) resulted in death, 15 (88.2%) required hospitalization, and 1 (5.9%) 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 TREPROSTINIL DIOLAMINE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does TREPROSTINIL DIOLAMINE Cause?
Headache (86)
Diarrhoea (68)
Dyspnoea (59)
Nausea (58)
Dizziness (34)
Flushing (28)
Vomiting (28)
Hypotension (26)
Dyspnoea exertional (25)
Malaise (25)
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 TREPROSTINIL DIOLAMINE Alternatives Have Lower Condition aggravated Risk?
TREPROSTINIL DIOLAMINE vs TRETINOIN
TREPROSTINIL DIOLAMINE vs TRIAMCINOLONE
TREPROSTINIL DIOLAMINE vs TRIAMCINOLONE ACETONIDE
TREPROSTINIL DIOLAMINE vs TRIAMCINOLONE HEXACETONIDE
TREPROSTINIL DIOLAMINE vs TRIAMTERENE