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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 MECASERMIN Cause Product dose omission? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product dose omission have been filed in association with MECASERMIN (GUNA-IGF). This represents 2.7% of all adverse event reports for MECASERMIN.

13
Reports of Product dose omission with MECASERMIN
2.7%
of all MECASERMIN reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product dose omission From MECASERMIN?

Of the 13 reports, 2 (15.4%) required hospitalization.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MECASERMIN. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does MECASERMIN Cause?

Off label use (117) Headache (41) Hypoglycaemia (36) Blood glucose decreased (32) Drug dose omission (27) Injection site pain (26) Vomiting (26) Fatigue (25) Pyrexia (23) Decreased appetite (22)

What Other Drugs Cause Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which MECASERMIN Alternatives Have Lower Product dose omission Risk?

MECASERMIN vs MECHLORETHAMINE MECASERMIN vs MECLIZINE MECASERMIN vs MEDROL MECASERMIN vs MEDROXYPROGESTERONE MECASERMIN vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE

Related Pages

MECASERMIN Full Profile All Product dose omission Reports All Drugs Causing Product dose omission MECASERMIN Demographics