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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FOLLITROPIN Cause Condition aggravated? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Condition aggravated have been filed in association with FOLLITROPIN (Gonal-f RFF Redi-ject). This represents 0.5% of all adverse event reports for FOLLITROPIN.

15
Reports of Condition aggravated with FOLLITROPIN
0.5%
of all FOLLITROPIN reports
0
Deaths
3
Hospitalizations

How Dangerous Is Condition aggravated From FOLLITROPIN?

Of the 15 reports, 3 (20.0%) required hospitalization, and 2 (13.3%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FOLLITROPIN. However, 15 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which FOLLITROPIN Alternatives Have Lower Condition aggravated Risk?

FOLLITROPIN vs FOLLITROPIN ALFA FOLLITROPIN vs FOLLITROPIN BETA FOLLITROPIN vs FOLLITROPIN\LUTEINIZING HORMONE FOLLITROPIN vs FOLLITROPIN\LUTROPIN ALFA FOLLITROPIN vs FONDAPARINUX

Related Pages

FOLLITROPIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated FOLLITROPIN Demographics