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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 LANREOTIDE Cause Product dose omission? 86 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 86 reports of Product dose omission have been filed in association with LANREOTIDE (Lanreotide Acetate). This represents 1.0% of all adverse event reports for LANREOTIDE.

86
Reports of Product dose omission with LANREOTIDE
1.0%
of all LANREOTIDE reports
3
Deaths
29
Hospitalizations

How Dangerous Is Product dose omission From LANREOTIDE?

Of the 86 reports, 3 (3.5%) resulted in death, 29 (33.7%) 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 LANREOTIDE. However, 86 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?

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 LANREOTIDE Alternatives Have Lower Product dose omission Risk?

LANREOTIDE vs LANSOPRAZOLE LANREOTIDE vs LANTHANUM LANREOTIDE vs LANTUS LANREOTIDE vs LANTUS SOLOSTAR LANREOTIDE vs LAPATINIB

Related Pages

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