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
120005666 12000566 6 F 20160115 20160912 20160204 20160915 EXP PHHY2016CA006992 NOVARTIS 72.29 YR F Y 0.00000 20160915 MD 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
120005666 12000566 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) U 21008 30 MG /month
120005666 12000566 2 C COTAZYM PANCRELIPASE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120005666 12000566 1 Pancreatic neuroendocrine tumour
120005666 12000566 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120005666 12000566 HO
120005666 12000566 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120005666 12000566 Aortic aneurysm
120005666 12000566 Blood pressure systolic increased
120005666 12000566 Cough
120005666 12000566 Dyspnoea
120005666 12000566 Fatigue
120005666 12000566 Influenza
120005666 12000566 Injection site pain
120005666 12000566 Lung neoplasm malignant
120005666 12000566 Malignant neoplasm of eye
120005666 12000566 Productive cough
120005666 12000566 Second primary malignancy

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
120005666 12000566 1 20071220 0