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
112035524 11203552 4 F 20121217 20160907 20150619 20160909 EXP PHHY2012CA041573 NOVARTIS 77.13 YR M Y 0.00000 20160909 CN 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
112035524 11203552 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (ONCE A MONTH) U 21008 30 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112035524 11203552 1 Neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
112035524 11203552 HO
112035524 11203552 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112035524 11203552 Back pain
112035524 11203552 Blood pressure increased
112035524 11203552 Blood pressure systolic increased
112035524 11203552 Delirium
112035524 11203552 Depression
112035524 11203552 Epilepsy
112035524 11203552 Fatigue
112035524 11203552 Gait disturbance
112035524 11203552 Injection site pain
112035524 11203552 Oedema peripheral
112035524 11203552 Pain
112035524 11203552 Spinal fracture

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
112035524 11203552 1 20111213 0