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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TREPROSTINIL Cause Full blood count abnormal? 25 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Full blood count abnormal have been filed in association with TREPROSTINIL (TYVASO). This represents 0.0% of all adverse event reports for TREPROSTINIL.

25
Reports of Full blood count abnormal with TREPROSTINIL
0.0%
of all TREPROSTINIL reports
5
Deaths
19
Hospitalizations

How Dangerous Is Full blood count abnormal From TREPROSTINIL?

Of the 25 reports, 5 (20.0%) resulted in death, 19 (76.0%) required hospitalization.

Is Full blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TREPROSTINIL. However, 25 reports have been filed with the FAERS database.

What Other Side Effects Does TREPROSTINIL Cause?

Dyspnoea (16,348) Headache (14,051) Diarrhoea (11,335) Nausea (10,320) Cough (8,945) Fatigue (7,440) Dizziness (7,405) Infusion site pain (5,169) Vomiting (5,097) Death (4,764)

What Other Drugs Cause Full blood count abnormal?

ALBUTEROL (3,060) PREDNISONE (2,230) BUDESONIDE\FORMOTEROL (1,786) TIOTROPIUM (1,754) MONTELUKAST (1,529) MEPOLIZUMAB (1,440) BUDESONIDE (1,339) PALBOCICLIB (1,146) CICLESONIDE (916) PANTOPRAZOLE (776)

Which TREPROSTINIL Alternatives Have Lower Full blood count abnormal Risk?

TREPROSTINIL vs TREPROSTINIL DIOLAMINE TREPROSTINIL vs TRETINOIN TREPROSTINIL vs TRIAMCINOLONE TREPROSTINIL vs TRIAMCINOLONE ACETONIDE TREPROSTINIL vs TRIAMCINOLONE HEXACETONIDE

Related Pages

TREPROSTINIL Full Profile All Full blood count abnormal Reports All Drugs Causing Full blood count abnormal TREPROSTINIL Demographics