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
123540572 12354057 2 F 20160628 20160511 20160704 EXP PHHY2015CA093148 NOVARTIS 0.00 M Y 0.00000 20160704 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
123540572 12354057 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, (EVERY 2 WEEKS) U 21008 30 MG QOW
123540572 12354057 2 C RAMIPRIL. RAMIPRIL 1 Unknown 10 MG, QD U 0 10 MG QD
123540572 12354057 3 C BISOPROLOL BISOPROLOL 1 Unknown 5 MG, QD U 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123540572 12354057 1 Neuroendocrine tumour
123540572 12354057 2 Product used for unknown indication
123540572 12354057 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123540572 12354057 HO
123540572 12354057 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123540572 12354057 Asthenia
123540572 12354057 Cachexia
123540572 12354057 Confusional state
123540572 12354057 Decreased appetite
123540572 12354057 Dyspnoea
123540572 12354057 Inappropriate schedule of drug administration
123540572 12354057 Oedema peripheral
123540572 12354057 Pain in extremity
123540572 12354057 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
123540572 12354057 1 20101115 0