Does DINOPROSTONE Cause Product quality issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product quality issue have been filed in association with DINOPROSTONE (CERVIDIL). This represents 0.7% of all adverse event reports for DINOPROSTONE.
5
Reports of Product quality issue with DINOPROSTONE
0.7%
of all DINOPROSTONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product quality issue From DINOPROSTONE?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DINOPROSTONE. However, 5 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which DINOPROSTONE Alternatives Have Lower Product quality issue Risk?
DINOPROSTONE vs DINUTUXIMAB
DINOPROSTONE vs DINUTUXIMAB BETA
DINOPROSTONE vs DIOSMIN
DINOPROSTONE vs DIOSMIN\HESPERIDIN
DINOPROSTONE vs DIOVAN