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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 INVEGA SUSTENNA Cause Condition aggravated? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Condition aggravated have been filed in association with INVEGA SUSTENNA. This represents 1.5% of all adverse event reports for INVEGA SUSTENNA.

10
Reports of Condition aggravated with INVEGA SUSTENNA
1.5%
of all INVEGA SUSTENNA reports
0
Deaths
4
Hospitalizations

How Dangerous Is Condition aggravated From INVEGA SUSTENNA?

Of the 10 reports, 4 (40.0%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for INVEGA SUSTENNA. However, 10 reports have been filed with the FAERS database.

What Other Side Effects Does INVEGA SUSTENNA Cause?

Drug dose omission (98) Drug ineffective (58) Inappropriate schedule of drug administration (39) Weight increased (34) Blood prolactin increased (27) Galactorrhoea (25) Injection site mass (20) Injection site nodule (19) Injection site pain (19) Investigation (17)

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 INVEGA SUSTENNA Alternatives Have Lower Condition aggravated Risk?

INVEGA SUSTENNA vs INVESTIGATIONAL BIOSIMILARS INVEGA SUSTENNA vs INVESTIGATIONAL PRODUCT INVEGA SUSTENNA vs INVOKANA INVEGA SUSTENNA vs IOBENGUANE I-131 INVEGA SUSTENNA vs IOBITRIDOL

Related Pages

INVEGA SUSTENNA Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated INVEGA SUSTENNA Demographics