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
113348872 11334887 2 F 20120928 20160822 20150804 20160825 EXP PHHY2011CA112250 NOVARTIS 81.93 YR F Y 0.00000 20160825 OT 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
113348872 11334887 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 60 MG, QMO 677.947998 MG N 21008 60 MG /month
113348872 11334887 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO 677.947998 MG N 21008 30 MG /month
113348872 11334887 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113348872 11334887 1 Neuroendocrine carcinoma metastatic
113348872 11334887 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
113348872 11334887 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113348872 11334887 Abdominal discomfort
113348872 11334887 Arthritis
113348872 11334887 Blood pressure increased
113348872 11334887 Decreased appetite
113348872 11334887 Diarrhoea
113348872 11334887 Drug intolerance
113348872 11334887 Dyspnoea
113348872 11334887 Headache
113348872 11334887 Malaise
113348872 11334887 Muscle spasms
113348872 11334887 Musculoskeletal stiffness
113348872 11334887 Myalgia
113348872 11334887 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
113348872 11334887 1 20111027 20160726 0
113348872 11334887 2 20160822 0