Does TRIMETHOPRIM Cause Product prescribing error? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product prescribing error have been filed in association with TRIMETHOPRIM (Trimethoprim). This represents 0.5% of all adverse event reports for TRIMETHOPRIM.
17
Reports of Product prescribing error with TRIMETHOPRIM
0.5%
of all TRIMETHOPRIM reports
0
Deaths
17
Hospitalizations
How Dangerous Is Product prescribing error From TRIMETHOPRIM?
Of the 17 reports, 17 (100.0%) required hospitalization, and 16 (94.1%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIMETHOPRIM. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does TRIMETHOPRIM Cause?
Headache (409)
Nausea (383)
Off label use (376)
Drug ineffective (368)
Malaise (346)
Swelling face (267)
Hypersensitivity (260)
Acute kidney injury (249)
Rash (235)
Drug intolerance (231)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which TRIMETHOPRIM Alternatives Have Lower Product prescribing error Risk?
TRIMETHOPRIM vs TRIMIPRAMINE
TRIMETHOPRIM vs TRIPROLIDINE
TRIMETHOPRIM vs TRIPTORELIN
TRIMETHOPRIM vs TRISODIUM
TRIMETHOPRIM vs TROFINETIDE