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
69929758 6992975 8 F 200902 20160628 20090513 20160701 EXP PHHY2008CA21011 NOVARTIS 81.99 YR F Y 0.00000 20160702 MD 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
69929758 6992975 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, EVERY 4 WEEKS U 21008 30 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
69929758 6992975 1 Carcinoid tumour

Outcome of event

Event ID CASEID OUTC COD
69929758 6992975 HO
69929758 6992975 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
69929758 6992975 Arthritis
69929758 6992975 Back injury
69929758 6992975 Back pain
69929758 6992975 Biliary dilatation
69929758 6992975 Blood pressure diastolic decreased
69929758 6992975 Blood pressure increased
69929758 6992975 Blood pressure systolic increased
69929758 6992975 Bone density decreased
69929758 6992975 Bone disorder
69929758 6992975 Cholelithiasis
69929758 6992975 Contusion
69929758 6992975 Diarrhoea
69929758 6992975 Fall
69929758 6992975 Fatigue
69929758 6992975 Femur fracture
69929758 6992975 Gait disturbance
69929758 6992975 Heart rate decreased
69929758 6992975 Hepatic lesion
69929758 6992975 Hip fracture
69929758 6992975 Limb injury
69929758 6992975 Lymphadenopathy
69929758 6992975 Pulmonary mass
69929758 6992975 Retroperitoneal lymphadenopathy
69929758 6992975 Sleep disorder

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
69929758 6992975 1 20080722 0