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
122004246 12200424 6 F 20160630 20160322 20160712 EXP PHHY2015CA155492 SANDOZ 0.00 F Y 0.00000 20160712 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
122004246 12200424 1 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO U 0 30 MG /month
122004246 12200424 2 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous 200 UG, BID (UNTIL LAR START) U 0 200 UG BID
122004246 12200424 3 PS METOPROLOL. METOPROLOL 1 Unknown 50 MG (IN MORNING) 100 MG (AT NIGHT) 73288

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122004246 12200424 1 Carcinoid tumour
122004246 12200424 2 Carcinoid tumour
122004246 12200424 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122004246 12200424 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122004246 12200424 Angina pectoris
122004246 12200424 Chest discomfort
122004246 12200424 Constipation
122004246 12200424 Dyspnoea
122004246 12200424 Gastrointestinal obstruction
122004246 12200424 General physical health deterioration

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
122004246 12200424 1 20151028 0
122004246 12200424 2 20150916 20151028 0