Does DINOPROSTONE Cause Haemoglobin decreased? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Haemoglobin decreased have been filed in association with DINOPROSTONE (CERVIDIL). This represents 4.3% of all adverse event reports for DINOPROSTONE.
31
Reports of Haemoglobin decreased with DINOPROSTONE
4.3%
of all DINOPROSTONE reports
0
Deaths
14
Hospitalizations
How Dangerous Is Haemoglobin decreased From DINOPROSTONE?
Of the 31 reports, 14 (45.2%) required hospitalization, and 1 (3.2%) 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 DINOPROSTONE. However, 31 reports have been filed with the FAERS database.
What Other Side Effects Does DINOPROSTONE Cause?
Foetal exposure during pregnancy (67)
Uterine hyperstimulation (65)
Off label use (52)
Premature separation of placenta (48)
Maternal exposure during pregnancy (46)
Postpartum haemorrhage (40)
Premature baby (40)
Drug ineffective (36)
Foetal heart rate deceleration abnormality (36)
Premature delivery (33)
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 DINOPROSTONE Alternatives Have Lower Haemoglobin decreased Risk?
DINOPROSTONE vs DINUTUXIMAB
DINOPROSTONE vs DINUTUXIMAB BETA
DINOPROSTONE vs DIOSMIN
DINOPROSTONE vs DIOSMIN\HESPERIDIN
DINOPROSTONE vs DIOVAN