Does LANREOTIDE Cause Product dose omission issue? 353 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 353 reports of Product dose omission issue have been filed in association with LANREOTIDE (Lanreotide Acetate). This represents 3.9% of all adverse event reports for LANREOTIDE.
353
Reports of Product dose omission issue with LANREOTIDE
3.9%
of all LANREOTIDE reports
39
Deaths
125
Hospitalizations
How Dangerous Is Product dose omission issue From LANREOTIDE?
Of the 353 reports, 39 (11.0%) resulted in death, 125 (35.4%) required hospitalization, and 6 (1.7%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LANREOTIDE. However, 353 reports have been filed with the FAERS database.
What Other Side Effects Does LANREOTIDE Cause?
Diarrhoea (1,646)
Off label use (1,536)
Death (1,177)
Fatigue (1,022)
Nausea (775)
Abdominal pain (662)
Injection site pain (618)
Malaise (520)
Headache (515)
Asthenia (483)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which LANREOTIDE Alternatives Have Lower Product dose omission issue Risk?
LANREOTIDE vs LANSOPRAZOLE
LANREOTIDE vs LANTHANUM
LANREOTIDE vs LANTUS
LANREOTIDE vs LANTUS SOLOSTAR
LANREOTIDE vs LAPATINIB