Does LEUPROLIDE Cause Respiratory distress? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Respiratory distress have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.0% of all adverse event reports for LEUPROLIDE.
23
Reports of Respiratory distress with LEUPROLIDE
0.0%
of all LEUPROLIDE reports
4
Deaths
22
Hospitalizations
How Dangerous Is Respiratory distress From LEUPROLIDE?
Of the 23 reports, 4 (17.4%) resulted in death, 22 (95.7%) required hospitalization, and 4 (17.4%) were considered life-threatening.
Is Respiratory distress Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does LEUPROLIDE Cause?
Hot flush (9,146)
Death (8,772)
Intercepted product preparation error (8,621)
Syringe issue (7,847)
Device leakage (5,861)
Wrong technique in product usage process (5,062)
Fatigue (4,805)
Injection site pain (4,678)
Prostatic specific antigen increased (2,432)
Asthenia (2,176)
What Other Drugs Cause Respiratory distress?
PREDNISONE (519)
CYCLOPHOSPHAMIDE (496)
METHOTREXATE (445)
DEXAMETHASONE (431)
RITUXIMAB (420)
TACROLIMUS (376)
ALBUTEROL (355)
TREPROSTINIL (345)
VINCRISTINE (342)
PREDNISOLONE (298)
Which LEUPROLIDE Alternatives Have Lower Respiratory distress Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM