Does SUMAVEL DOSEPRO Cause Incorrect dose administered by device? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Incorrect dose administered by device have been filed in association with SUMAVEL DOSEPRO. This represents 13.3% of all adverse event reports for SUMAVEL DOSEPRO.
49
Reports of Incorrect dose administered by device with SUMAVEL DOSEPRO
13.3%
of all SUMAVEL DOSEPRO reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect dose administered by device From SUMAVEL DOSEPRO?
Of the 49 reports.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUMAVEL DOSEPRO. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does SUMAVEL DOSEPRO Cause?
Injection site pain (151)
Device malfunction (96)
Injection site haemorrhage (88)
Accidental exposure to product (73)
Injection site bruising (68)
Drug ineffective (59)
Injection site urticaria (51)
Drug effect incomplete (38)
Injection site erythema (27)
Nausea (24)
What Other Drugs Cause Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which SUMAVEL DOSEPRO Alternatives Have Lower Incorrect dose administered by device Risk?
SUMAVEL DOSEPRO vs SUNITINIB
SUMAVEL DOSEPRO vs SUNITINIB MALATE
SUMAVEL DOSEPRO vs SUTENT
SUMAVEL DOSEPRO vs SUTIMLIMAB-JOME
SUMAVEL DOSEPRO vs SUVOREXANT