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
123808932 12380893 2 F 201504 20160816 20160518 20160819 EXP PHHY2015PA097439 NOVARTIS 71.78 YR M Y 0.00000 20160819 CN COUNTRY NOT SPECIFIED PA

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
123808932 12380893 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, QMO U 21008 40 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123808932 12380893 1 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
123808932 12380893 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123808932 12380893 Abasia
123808932 12380893 Abdominal mass
123808932 12380893 Ascites
123808932 12380893 Asthenia
123808932 12380893 Chills
123808932 12380893 Dyspnoea
123808932 12380893 Fall
123808932 12380893 Fatigue
123808932 12380893 General physical health deterioration
123808932 12380893 Generalised oedema
123808932 12380893 Hallucination
123808932 12380893 Injection site pain
123808932 12380893 Limb discomfort
123808932 12380893 Oliguria
123808932 12380893 Peripheral swelling
123808932 12380893 Skin exfoliation

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

no results found

Therapies reported

no results found