Does PENTOXIFYLLINE Cause Intentional product misuse? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Intentional product misuse have been filed in association with PENTOXIFYLLINE (Pentoxifylline). This represents 2.3% of all adverse event reports for PENTOXIFYLLINE.
33
Reports of Intentional product misuse with PENTOXIFYLLINE
2.3%
of all PENTOXIFYLLINE reports
1
Deaths
32
Hospitalizations
How Dangerous Is Intentional product misuse From PENTOXIFYLLINE?
Of the 33 reports, 1 (3.0%) resulted in death, 32 (97.0%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PENTOXIFYLLINE. However, 33 reports have been filed with the FAERS database.
What Other Side Effects Does PENTOXIFYLLINE Cause?
Fatigue (263)
Diarrhoea (262)
Insomnia (257)
Dizziness (247)
Fall (247)
Sepsis (242)
Pruritus (230)
Haemorrhagic stroke (226)
Chills (225)
Tachycardia (222)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which PENTOXIFYLLINE Alternatives Have Lower Intentional product misuse Risk?
PENTOXIFYLLINE vs PERAMIVIR
PENTOXIFYLLINE vs PERAMPANEL
PENTOXIFYLLINE vs PERAZINE
PENTOXIFYLLINE vs PERCOCET
PENTOXIFYLLINE vs PERFLUOROHEXYLOCTANE