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
91168516 9116851 6 F 201302 20160713 20130225 20160718 EXP PHHY2013CA010870 NOVARTIS 53.53 YR M Y 0.00000 20160717 OT 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
91168516 9116851 1 PS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous 100 UG, TID U 19667 100 UG TID
91168516 9116851 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (ONCE A MONTH) U S0098C 0 30 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91168516 9116851 1 Acral overgrowth
91168516 9116851 2 Acral overgrowth

Outcome of event

Event ID CASEID OUTC COD
91168516 9116851 HO
91168516 9116851 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
91168516 9116851 Abdominal pain
91168516 9116851 Abdominal pain upper
91168516 9116851 Blood pressure systolic increased
91168516 9116851 Blood prolactin abnormal
91168516 9116851 Brain neoplasm
91168516 9116851 Cerebrospinal fluid leakage
91168516 9116851 Diabetes mellitus
91168516 9116851 Heart rate decreased
91168516 9116851 Hormone level abnormal
91168516 9116851 Memory impairment
91168516 9116851 Nausea
91168516 9116851 Needle issue

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
91168516 9116851 1 20121215 0
91168516 9116851 2 20130328 0