Does TADALAFIL Cause Device occlusion? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Device occlusion have been filed in association with TADALAFIL (Esokalli Testosterone Booster Oral Dissolving Film). This represents 0.1% of all adverse event reports for TADALAFIL.
22
Reports of Device occlusion with TADALAFIL
0.1%
of all TADALAFIL reports
1
Deaths
19
Hospitalizations
How Dangerous Is Device occlusion From TADALAFIL?
Of the 22 reports, 1 (4.5%) resulted in death, 19 (86.4%) required hospitalization, and 2 (9.1%) were considered life-threatening.
Is Device occlusion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TADALAFIL. However, 22 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 Device occlusion?
PEGFILGRASTIM (3,239)
CARBIDOPA\LEVODOPA (1,464)
SOMATROPIN (823)
LEUPROLIDE (786)
EPOPROSTENOL (580)
TREPROSTINIL (458)
ALBUTEROL (431)
MEDROXYPROGESTERONE (284)
BACLOFEN (254)
LEVODOPA (224)
Which TADALAFIL Alternatives Have Lower Device occlusion Risk?
TADALAFIL vs TAFAMIDIS
TADALAFIL vs TAFAMIDIS MEGLUMINE
TADALAFIL vs TAFASITAMAB
TADALAFIL vs TAFASITAMAB-CXIX
TADALAFIL vs TAFINLAR