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
117572846 11757284 6 F 20130805 20160710 20151120 20160713 EXP PHHY2013CA085930 NOVARTIS 79.75 YR M Y 0.00000 20160713 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
117572846 11757284 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO U 21008 30 MG /month
117572846 11757284 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 60 MG, QMO (ONCE A MONTH) U 21008 60 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117572846 11757284 1 Neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
117572846 11757284 OT
117572846 11757284 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117572846 11757284 Blood glucose increased
117572846 11757284 Blood pressure increased
117572846 11757284 Blood pressure systolic increased
117572846 11757284 Body temperature increased
117572846 11757284 Chills
117572846 11757284 Dizziness
117572846 11757284 Dyspnoea
117572846 11757284 Heart rate increased
117572846 11757284 Influenza
117572846 11757284 Oedema peripheral
117572846 11757284 Pyrexia
117572846 11757284 Respiratory rate increased
117572846 11757284 Waist circumference increased

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
117572846 11757284 1 20130610 0