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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 Application site pruritus? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Application site pruritus have been filed in association with TADALAFIL (Esokalli Testosterone Booster Oral Dissolving Film). This represents 0.0% of all adverse event reports for TADALAFIL.

7
Reports of Application site pruritus with TADALAFIL
0.0%
of all TADALAFIL reports
0
Deaths
3
Hospitalizations

How Dangerous Is Application site pruritus From TADALAFIL?

Of the 7 reports, 3 (42.9%) required hospitalization.

Is Application site pruritus Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TADALAFIL. However, 7 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 Application site pruritus?

MINOXIDIL (3,727) NICOTINE (2,074) BUPRENORPHINE (1,687) ESTRADIOL (1,181) SUMATRIPTAN (675) FENTANYL (501) ESTRADIOL\NORETHINDRONE (463) CLONIDINE (335) ROTIGOTINE (334) INGENOL MEBUTATE (291)

Which TADALAFIL Alternatives Have Lower Application site pruritus Risk?

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

Related Pages

TADALAFIL Full Profile All Application site pruritus Reports All Drugs Causing Application site pruritus TADALAFIL Demographics