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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 SOMATROGON-GHLA Cause Device use error? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device use error have been filed in association with SOMATROGON-GHLA. This represents 0.5% of all adverse event reports for SOMATROGON-GHLA.

5
Reports of Device use error with SOMATROGON-GHLA
0.5%
of all SOMATROGON-GHLA reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device use error From SOMATROGON-GHLA?

Of the 5 reports.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOMATROGON-GHLA. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does SOMATROGON-GHLA Cause?

Injection site pain (738) Wrong technique in device usage process (43) Injection site erythema (42) Incorrect dose administered by device (41) Injection site swelling (38) Off label use (29) Patient-device incompatibility (29) Headache (27) Needle issue (27) Device mechanical issue (24)

What Other Drugs Cause Device use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which SOMATROGON-GHLA Alternatives Have Lower Device use error Risk?

SOMATROGON-GHLA vs SOMATROPIN SOMATROGON-GHLA vs SPIRAMYCIN SOMATROGON-GHLA vs SUFENTANIL SOMATROGON-GHLA vs SULBACTAM SOMATROGON-GHLA vs SULFAMETHOXAZOLE\TRIMETHOPRIM

Related Pages

SOMATROGON-GHLA Full Profile All Device use error Reports All Drugs Causing Device use error SOMATROGON-GHLA Demographics