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
104725079 10472507 9 F 20130502 20160914 20140924 20160920 EXP PHHY2012CA033545 NOVARTIS 62.44 YR M Y 0.00000 20160920 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
104725079 10472507 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, EVERY 3 WEEKS U 21008 30 MG Q3W
104725079 10472507 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, EVERY 3 WEEKS U 21008 40 MG Q3W

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104725079 10472507 1 Pancreatitis chronic

Outcome of event

Event ID CASEID OUTC COD
104725079 10472507 OT
104725079 10472507 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104725079 10472507 Abdominal pain
104725079 10472507 Abdominal pain upper
104725079 10472507 Blood pressure decreased
104725079 10472507 Blood pressure increased
104725079 10472507 Bronchitis
104725079 10472507 Cardiac disorder
104725079 10472507 Diarrhoea
104725079 10472507 Inappropriate schedule of drug administration
104725079 10472507 Lung disorder
104725079 10472507 Malaise
104725079 10472507 Pancreatic neoplasm
104725079 10472507 Pneumonia
104725079 10472507 Product use issue
104725079 10472507 Secretion discharge
104725079 10472507 Weight decreased

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
104725079 10472507 1 20111006 0