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
109317734 10931773 4 F 20160723 20160727 20150319 20160803 EXP PHHY2015AU027688 NOVARTIS 82.11 YR M Y 0.00000 20160803 CN COUNTRY NOT SPECIFIED AU

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
109317734 10931773 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG U S0287,S0046,347407, 349238,350145 21008 40 MG SUSPENSION
109317734 10931773 2 C WARFARIN WARFARIN 1 Unknown U 0
109317734 10931773 3 C METOPROLOL. METOPROLOL 1 Unknown 25 MG U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109317734 10931773 1 Carcinoid syndrome
109317734 10931773 2 International normalised ratio abnormal
109317734 10931773 3 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
109317734 10931773 OT
109317734 10931773 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109317734 10931773 Blood glucose increased
109317734 10931773 Body temperature increased
109317734 10931773 Impaired healing
109317734 10931773 Infected skin ulcer
109317734 10931773 Malaise
109317734 10931773 Second primary malignancy
109317734 10931773 Skin cancer
109317734 10931773 Skin ulcer
109317734 10931773 Urinary bladder haemorrhage
109317734 10931773 Urinary retention

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found