Does FOLLITROPIN Cause Poor quality device used? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Poor quality device used have been filed in association with FOLLITROPIN (Gonal-f RFF Redi-ject). This represents 2.1% of all adverse event reports for FOLLITROPIN.
58
Reports of Poor quality device used with FOLLITROPIN
2.1%
of all FOLLITROPIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Poor quality device used From FOLLITROPIN?
Of the 58 reports.
Is Poor quality device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOLLITROPIN. However, 58 reports have been filed with the FAERS database.
What Other Side Effects Does FOLLITROPIN Cause?
Ovarian hyperstimulation syndrome (718)
Ascites (213)
No adverse event (213)
Abdominal distension (154)
Headache (151)
Nausea (129)
Abdominal pain (115)
Product quality issue (111)
Abortion spontaneous (102)
Dyspnoea (101)
What Other Drugs Cause Poor quality device used?
SOMATROPIN (3,162)
MOMETASONE FUROATE (2,159)
ALBUTEROL (1,251)
FORMOTEROL\MOMETASONE FUROATE (1,091)
MEDROXYPROGESTERONE (80)
ETHINYL ESTRADIOL\ETONOGESTREL (77)
ETONOGESTREL (55)
ETANERCEPT (46)
ESTRADIOL (41)
PEGFILGRASTIM (38)
Which FOLLITROPIN Alternatives Have Lower Poor quality device used Risk?
FOLLITROPIN vs FOLLITROPIN ALFA
FOLLITROPIN vs FOLLITROPIN BETA
FOLLITROPIN vs FOLLITROPIN\LUTEINIZING HORMONE
FOLLITROPIN vs FOLLITROPIN\LUTROPIN ALFA
FOLLITROPIN vs FONDAPARINUX