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
111756684 11175668 4 F 20150603 20160712 20150609 20160718 EXP PHHY2015CA068245 NOVARTIS 59.48 YR F Y 0.00000 20160718 CN COUNTRY NOT SPECIFIED 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
111756684 11175668 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, EVERY 4 WEEKS U 21008 30 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111756684 11175668 1 Metastatic carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
111756684 11175668 HO
111756684 11175668 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111756684 11175668 Abdominal discomfort
111756684 11175668 Alopecia
111756684 11175668 Decreased appetite
111756684 11175668 Malignant neoplasm progression
111756684 11175668 Metastases to chest wall
111756684 11175668 Metastases to spine
111756684 11175668 Pain
111756684 11175668 Terminal state
111756684 11175668 Weight decreased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
111756684 11175668 1 20150528 0