Does TRIHEPTANOIN Cause Product preparation error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product preparation error have been filed in association with TRIHEPTANOIN (DOJOLVI). This represents 1.4% of all adverse event reports for TRIHEPTANOIN.
7
Reports of Product preparation error with TRIHEPTANOIN
1.4%
of all TRIHEPTANOIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product preparation error From TRIHEPTANOIN?
Of the 7 reports, 2 (28.6%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIHEPTANOIN. However, 7 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 Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which TRIHEPTANOIN Alternatives Have Lower Product preparation error Risk?
TRIHEPTANOIN vs TRIHEXYPHENIDYL
TRIHEPTANOIN vs TRILACICLIB
TRIHEPTANOIN vs TRILEPTAL
TRIHEPTANOIN vs TRIMEBUTINE
TRIHEPTANOIN vs TRIMEPRAZINE