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
105258065 10525806 5 F 20141029 20160719 20141017 20160722 EXP PHHY2011CA68947 NOVARTIS 59.93 YR F Y 0.00000 20160722 CN 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
105258065 10525806 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) 21008 30 MG /month
105258065 10525806 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 60 MG, QMO (EVERY 4 WEEKS) 21008 60 MG /month
105258065 10525806 3 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous 500 UG, PRN 0 500 UG
105258065 10525806 4 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous 50 MG, TID 0 50 MG TID
105258065 10525806 5 C IMOVANE ZOPICLONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105258065 10525806 1 Neuroendocrine tumour
105258065 10525806 3 Neuroendocrine tumour
105258065 10525806 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105258065 10525806 HO
105258065 10525806 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105258065 10525806 Abdominal pain upper
105258065 10525806 Body temperature decreased
105258065 10525806 Bursitis
105258065 10525806 Cholelithiasis
105258065 10525806 Flushing
105258065 10525806 Gastrooesophageal reflux disease
105258065 10525806 Pneumothorax
105258065 10525806 Venous injury

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
105258065 10525806 1 20110419 0
105258065 10525806 3 20140123 0