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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 TRIHEPTANOIN Cause Condition aggravated? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Condition aggravated have been filed in association with TRIHEPTANOIN (DOJOLVI). This represents 2.0% of all adverse event reports for TRIHEPTANOIN.

10
Reports of Condition aggravated with TRIHEPTANOIN
2.0%
of all TRIHEPTANOIN reports
4
Deaths
6
Hospitalizations

How Dangerous Is Condition aggravated From TRIHEPTANOIN?

Of the 10 reports, 4 (40.0%) resulted in death, 6 (60.0%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRIHEPTANOIN. However, 10 reports have been filed with the FAERS database.

What Other Side Effects Does TRIHEPTANOIN Cause?

Vomiting (79) Diarrhoea (70) Rhabdomyolysis (53) Off label use (48) Abdominal pain upper (38) Abdominal discomfort (34) Blood creatine phosphokinase increased (34) Death (29) Nausea (26) Gastrointestinal disorder (23)

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 TRIHEPTANOIN Alternatives Have Lower Condition aggravated Risk?

TRIHEPTANOIN vs TRIHEXYPHENIDYL TRIHEPTANOIN vs TRILACICLIB TRIHEPTANOIN vs TRILEPTAL TRIHEPTANOIN vs TRIMEBUTINE TRIHEPTANOIN vs TRIMEPRAZINE

Related Pages

TRIHEPTANOIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated TRIHEPTANOIN Demographics