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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 Tonsillar hypertrophy? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Tonsillar hypertrophy have been filed in association with MECASERMIN (GUNA-IGF). This represents 4.6% of all adverse event reports for MECASERMIN.

22
Reports of Tonsillar hypertrophy with MECASERMIN
4.6%
of all MECASERMIN reports
0
Deaths
7
Hospitalizations

How Dangerous Is Tonsillar hypertrophy From MECASERMIN?

Of the 22 reports, 7 (31.8%) required hospitalization, and 1 (4.5%) were considered life-threatening.

Is Tonsillar hypertrophy Listed in the Official Label?

Yes, Tonsillar hypertrophy is listed as a known adverse reaction in the official FDA drug label for MECASERMIN.

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 Tonsillar hypertrophy?

ADALIMUMAB (151) ONDANSETRON (51) SOMATROPIN (43) SECUKINUMAB (42) DUPILUMAB (39) METHOTREXATE (39) INFLIXIMAB (31) TACROLIMUS (26) INFLIXIMAB-DYYB (25) ETANERCEPT (24)

Which MECASERMIN Alternatives Have Lower Tonsillar hypertrophy Risk?

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

Related Pages

MECASERMIN Full Profile All Tonsillar hypertrophy Reports All Drugs Causing Tonsillar hypertrophy MECASERMIN Demographics