The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125565811 12556581 1 I 20160708 20160714 20160714 EXP CA-IPSEN BIOPHARMACEUTICALS, INC.-2016-06002 IPSEN 0.00 F Y 0.00000 20160714 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125565811 12556581 1 PS SOMATULINE AUTOGEL LANREOTIDE ACETATE 1 Subcutaneous 120 MG U 0 120 MG SOLUTION FOR INJECTION/INFUSION QOW
125565811 12556581 2 SS OCTREOTIDE ACETATE. OCTREOTIDE ACETATE 1 Subcutaneous 0
125565811 12556581 3 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 0 60 MG QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125565811 12556581 1 Carcinoid syndrome
125565811 12556581 2 Carcinoid syndrome
125565811 12556581 3 Carcinoid syndrome

Outcome of event

Event ID CASEID OUTC COD
125565811 12556581 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125565811 12556581 Calcification of muscle
125565811 12556581 Dehydration
125565811 12556581 Diarrhoea
125565811 12556581 Inappropriate schedule of drug administration
125565811 12556581 Intestinal obstruction

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found