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
115124493 11512449 3 F 20160913 20150916 20160919 EXP PHHY2015BR111293 NOVARTIS 0.00 M Y 85.00000 KG 20160919 MD BR BR

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
115124493 11512449 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Unknown 20 MG, QMO (EVERY 28 DAYS) U 21008 20 MG AMPOULE /month
115124493 11512449 2 C CARVEDILOL. CARVEDILOL 1 Unknown U 0
115124493 11512449 3 C SIMVASTATIN. SIMVASTATIN 1 Unknown U 0
115124493 11512449 4 C VASTAREL TRIMETAZIDINE DIHYDROCHLORIDE 1 Unknown U 0
115124493 11512449 5 C ASA ASPIRIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115124493 11512449 1 Neuroendocrine tumour
115124493 11512449 2 Product used for unknown indication
115124493 11512449 3 Product used for unknown indication
115124493 11512449 4 Product used for unknown indication
115124493 11512449 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
115124493 11512449 OT
115124493 11512449 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115124493 11512449 Embolism venous
115124493 11512449 Gait disturbance
115124493 11512449 Hepatic failure
115124493 11512449 Hepatic neoplasm
115124493 11512449 Hepatic pain
115124493 11512449 Hepatitis
115124493 11512449 Hypertension
115124493 11512449 Pain in extremity

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
115124493 11512449 1 2012 0