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
105109089 10510908 9 F 20140710 20160725 20141010 20160801 EXP PHHY2014AU085041 NOVARTIS 56.93 YR F Y 0.00000 20160801 CN COUNTRY NOT SPECIFIED AU

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
105109089 10510908 1 PS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous U 19667
105109089 10510908 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG U 345406,345941,346714,347407, S0310 0 30 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105109089 10510908 1 Product used for unknown indication
105109089 10510908 2 Carcinoid syndrome

Outcome of event

Event ID CASEID OUTC COD
105109089 10510908 HO
105109089 10510908 OT
105109089 10510908 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
105109089 10510908 Diarrhoea
105109089 10510908 Dyspnoea
105109089 10510908 Fluid retention
105109089 10510908 Flushing
105109089 10510908 Gingivitis
105109089 10510908 Heart rate irregular
105109089 10510908 International normalised ratio abnormal
105109089 10510908 Needle issue
105109089 10510908 Palpitations
105109089 10510908 Post procedural haemorrhage
105109089 10510908 Supraventricular tachycardia
105109089 10510908 Tachycardia
105109089 10510908 Tooth fracture
105109089 10510908 Tricuspid valve calcification
105109089 10510908 Tricuspid valve incompetence
105109089 10510908 Tricuspid valve stenosis
105109089 10510908 Weight decreased

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

no results found

Therapies reported

no results found