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
94796074 9479607 4 F 2013 20160920 20130827 20160926 EXP PHHY2013CA078479 NOVARTIS 66.63 YR F Y 0.00000 20160926 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
94796074 9479607 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) U 21008 30 MG SUSPENSION /month
94796074 9479607 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 U 21008 SUSPENSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94796074 9479607 1 Neuroendocrine tumour
94796074 9479607 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
94796074 9479607 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
94796074 9479607 Abdominal distension
94796074 9479607 Abdominal pain
94796074 9479607 Abdominal pain upper
94796074 9479607 Ascites
94796074 9479607 Blood pressure diastolic decreased
94796074 9479607 Blood pressure increased
94796074 9479607 Dyspepsia
94796074 9479607 Flatulence
94796074 9479607 Heart rate 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
94796074 9479607 1 20130502 0