Does FOLLITROPIN Cause Product container issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product container issue have been filed in association with FOLLITROPIN (Gonal-f RFF Redi-ject). This represents 0.3% of all adverse event reports for FOLLITROPIN.
8
Reports of Product container issue with FOLLITROPIN
0.3%
of all FOLLITROPIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From FOLLITROPIN?
Of the 8 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOLLITROPIN. However, 8 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 Product container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
Which FOLLITROPIN Alternatives Have Lower Product container issue Risk?
FOLLITROPIN vs FOLLITROPIN ALFA
FOLLITROPIN vs FOLLITROPIN BETA
FOLLITROPIN vs FOLLITROPIN\LUTEINIZING HORMONE
FOLLITROPIN vs FOLLITROPIN\LUTROPIN ALFA
FOLLITROPIN vs FONDAPARINUX