Does PHENPROCOUMON Cause Product prescribing error? 104 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 104 reports of Product prescribing error have been filed in association with PHENPROCOUMON. This represents 7.5% of all adverse event reports for PHENPROCOUMON.
104
Reports of Product prescribing error with PHENPROCOUMON
7.5%
of all PHENPROCOUMON reports
4
Deaths
101
Hospitalizations
How Dangerous Is Product prescribing error From PHENPROCOUMON?
Of the 104 reports, 4 (3.8%) resulted in death, 101 (97.1%) required hospitalization, and 17 (16.3%) 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 PHENPROCOUMON. However, 104 reports have been filed with the FAERS database.
What Other Side Effects Does PHENPROCOUMON Cause?
Anaemia (242)
General physical health deterioration (172)
Haematochezia (162)
Dyspnoea (140)
Gastrointestinal haemorrhage (122)
Overdose (109)
Dizziness (108)
Haematoma (108)
Fall (92)
International normalised ratio increased (81)
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 PHENPROCOUMON Alternatives Have Lower Product prescribing error Risk?
PHENPROCOUMON vs PHENTERMINE
PHENPROCOUMON vs PHENTERMINE\TOPIRAMATE
PHENPROCOUMON vs PHENTOLAMINE
PHENPROCOUMON vs PHENYLEPHRINE
PHENPROCOUMON vs PHENYLEPHRINE\PHENYLEPHRINE