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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 TADALAFIL Cause Intentional product misuse? 517 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 517 reports of Intentional product misuse have been filed in association with TADALAFIL (Esokalli Testosterone Booster Oral Dissolving Film). This represents 1.7% of all adverse event reports for TADALAFIL.

517
Reports of Intentional product misuse with TADALAFIL
1.7%
of all TADALAFIL reports
17
Deaths
37
Hospitalizations

How Dangerous Is Intentional product misuse From TADALAFIL?

Of the 517 reports, 17 (3.3%) resulted in death, 37 (7.2%) required hospitalization, and 5 (1.0%) were considered life-threatening.

Is Intentional product misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TADALAFIL. However, 517 reports have been filed with the FAERS database.

What Other Side Effects Does TADALAFIL Cause?

Headache (3,196) Drug ineffective (2,943) Dyspnoea (2,881) Death (1,917) Diarrhoea (1,667) Dizziness (1,374) Nausea (1,368) Asthenia (1,230) Fatigue (1,135) Hypertension (1,044)

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 TADALAFIL Alternatives Have Lower Intentional product misuse Risk?

TADALAFIL vs TAFAMIDIS TADALAFIL vs TAFAMIDIS MEGLUMINE TADALAFIL vs TAFASITAMAB TADALAFIL vs TAFASITAMAB-CXIX TADALAFIL vs TAFINLAR

Related Pages

TADALAFIL Full Profile All Intentional product misuse Reports All Drugs Causing Intentional product misuse TADALAFIL Demographics