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
990323210 9903232 10 F 2013 20160915 20140217 20160923 EXP PHHY2013CA070468 SANDOZ 87.83 YR M Y 0.00000 20160923 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
990323210 9903232 1 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO D 0 30 MG SUSPENSION /month
990323210 9903232 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO D 0 30 MG SUSPENSION /month
990323210 9903232 3 PS METOPROLOL. METOPROLOL 1 Unknown D 73288 MODIFIED RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
990323210 9903232 1 Carcinoid tumour
990323210 9903232 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
990323210 9903232 HO
990323210 9903232 OT
990323210 9903232 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
990323210 9903232 Back pain
990323210 9903232 Blood pressure increased
990323210 9903232 Confusional state
990323210 9903232 Diarrhoea
990323210 9903232 Fall
990323210 9903232 Memory impairment
990323210 9903232 Mobility decreased
990323210 9903232 Pelvic fracture
990323210 9903232 Pleural effusion
990323210 9903232 Pneumonia

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
990323210 9903232 1 20120524 0
990323210 9903232 2 20140411 0