Does LEUPROLIDE Cause Haemoglobin decreased? 279 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 279 reports of Haemoglobin decreased have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.4% of all adverse event reports for LEUPROLIDE.
279
Reports of Haemoglobin decreased with LEUPROLIDE
0.4%
of all LEUPROLIDE reports
39
Deaths
130
Hospitalizations
How Dangerous Is Haemoglobin decreased From LEUPROLIDE?
Of the 279 reports, 39 (14.0%) resulted in death, 130 (46.6%) required hospitalization, and 3 (1.1%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 279 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which LEUPROLIDE Alternatives Have Lower Haemoglobin decreased Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM