Does FOLLITROPIN Cause Product quality issue? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Product quality issue have been filed in association with FOLLITROPIN (Gonal-f RFF Redi-ject). This represents 4.0% of all adverse event reports for FOLLITROPIN.
111
Reports of Product quality issue with FOLLITROPIN
4.0%
of all FOLLITROPIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From FOLLITROPIN?
Of the 111 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOLLITROPIN. However, 111 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)
Abortion spontaneous (102)
Dyspnoea (101)
Incorrect dose administered (86)
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 FOLLITROPIN Alternatives Have Lower Product quality issue Risk?
FOLLITROPIN vs FOLLITROPIN ALFA
FOLLITROPIN vs FOLLITROPIN BETA
FOLLITROPIN vs FOLLITROPIN\LUTEINIZING HORMONE
FOLLITROPIN vs FOLLITROPIN\LUTROPIN ALFA
FOLLITROPIN vs FONDAPARINUX