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
95185649 9518564 9 F 20111228 20160704 20130912 20160711 EXP PHHY2011CA114593 NOVARTIS 48.91 YR F Y 0.00000 20160711 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
95185649 9518564 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 20 MG, QMO (EVERY 4 WEEKS) U 21008 20 MG /month
95185649 9518564 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO U 21008 30 MG /month
95185649 9518564 3 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular UNK U 21008
95185649 9518564 4 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, ONCE A MONTH U 21008 30 MG /month
95185649 9518564 5 C COUMADIN WARFARIN SODIUM 1 Unknown UNK Y 0
95185649 9518564 6 C CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK U 0
95185649 9518564 7 C REOMEN 2 Unknown UNK U 0
95185649 9518564 8 C VITAMIN D CHOLECALCIFEROL 1 Unknown UNK U 0
95185649 9518564 9 C CALCIUM CALCIUM 1 Unknown UNK U 0
95185649 9518564 10 C VITAMIN K NOS 2 Unknown UNK U 0
95185649 9518564 11 C IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown UNK U 0
95185649 9518564 12 C PANTOLOC CONTROL 2 Unknown UNK U 0
95185649 9518564 13 C CORTEF HYDROCORTISONE 1 Unknown UNK U 0
95185649 9518564 14 C CODEINE CODEINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
95185649 9518564 1 Crohn's disease
95185649 9518564 5 Product used for unknown indication
95185649 9518564 6 Product used for unknown indication
95185649 9518564 7 Product used for unknown indication
95185649 9518564 8 Product used for unknown indication
95185649 9518564 9 Product used for unknown indication
95185649 9518564 10 Product used for unknown indication
95185649 9518564 11 Product used for unknown indication
95185649 9518564 12 Product used for unknown indication
95185649 9518564 13 Product used for unknown indication
95185649 9518564 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
95185649 9518564 OT
95185649 9518564 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
95185649 9518564 Abdominal pain upper
95185649 9518564 Body temperature decreased
95185649 9518564 Endometrial cancer stage IV
95185649 9518564 Epistaxis
95185649 9518564 Heart rate decreased
95185649 9518564 Injection site induration
95185649 9518564 Injection site pain
95185649 9518564 Pain
95185649 9518564 Product use issue
95185649 9518564 Renal cell carcinoma
95185649 9518564 Renal neoplasm

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
95185649 9518564 1 20111228 0
95185649 9518564 3 20131202 0