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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 SOMATROPIN Cause Product solubility abnormal? 98 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Product solubility abnormal have been filed in association with SOMATROPIN (Nutropin AQ NuSpin 10). This represents 0.1% of all adverse event reports for SOMATROPIN.

98
Reports of Product solubility abnormal with SOMATROPIN
0.1%
of all SOMATROPIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product solubility abnormal From SOMATROPIN?

Of the 98 reports.

Is Product solubility abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SOMATROPIN. However, 98 reports have been filed with the FAERS database.

What Other Side Effects Does SOMATROPIN Cause?

Drug dose omission by device (15,921) Device leakage (9,113) Device breakage (7,761) Device mechanical issue (6,411) Device information output issue (5,220) Device issue (5,131) Wrong technique in device usage process (4,746) Injection site pain (4,009) Poor quality device used (3,162) Device use error (2,801)

What Other Drugs Cause Product solubility abnormal?

BUPRENORPHINE (498) BUPRENORPHINE\NALOXONE (274) POLYETHYLENE GLYCOL 3350 (220) CHOLESTYRAMINE (193) PATIROMER (107) LEVOTHYROXINE (100) EXENATIDE (97) ESTRADIOL (94) NITROGLYCERIN (81) AMLODIPINE (76)

Which SOMATROPIN Alternatives Have Lower Product solubility abnormal Risk?

SOMATROPIN vs SONIDEGIB SOMATROPIN vs SORAFENIB SOMATROPIN vs SORGHUM HALEPENSE POLLEN SOMATROPIN vs SOTAGLIFLOZIN SOMATROPIN vs SOTALOL

Related Pages

SOMATROPIN Full Profile All Product solubility abnormal Reports All Drugs Causing Product solubility abnormal SOMATROPIN Demographics