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
97971709 9797170 9 F 20131111 20160831 20140106 20160906 EXP PHHY2013IL130164 NOVARTIS 78.37 YR M Y 85.00000 KG 20160906 CN IL IL

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
97971709 9797170 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, EVERY FOUR WEEK (Q4W) U SO053, SO309 21008 40 MG /month
97971709 9797170 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, QMO U 0246, S0252, SO046, SO267/SO047/SO 21008 40 MG /month
97971709 9797170 3 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 60 MG, QMO U S0324 21008 60 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97971709 9797170 1 Carcinoid tumour
97971709 9797170 2 Neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
97971709 9797170 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97971709 9797170 Abdominal pain
97971709 9797170 Anal incontinence
97971709 9797170 Asthenia
97971709 9797170 Diarrhoea
97971709 9797170 Erythema
97971709 9797170 Fall
97971709 9797170 Feeling abnormal
97971709 9797170 Flushing
97971709 9797170 Heart rate decreased
97971709 9797170 Hyperhidrosis
97971709 9797170 Hypoglycaemia
97971709 9797170 Hypotension
97971709 9797170 Loss of consciousness
97971709 9797170 Nausea
97971709 9797170 Pruritus
97971709 9797170 Pruritus generalised
97971709 9797170 Rash
97971709 9797170 Rash generalised
97971709 9797170 Sensory loss
97971709 9797170 Skin burning sensation
97971709 9797170 Syncope

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
97971709 9797170 1 20130603 0
97971709 9797170 3 20160831 0