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
78917869 7891786 9 F 20130903 20160902 20110408 20160908 EXP PHHY2011CA25382 NOVARTIS 77.49 YR M Y 0.00000 20160908 CN COUNTRY NOT SPECIFIED 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
78917869 7891786 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, QMO (ONCE A MONTH) U 21008 40 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
78917869 7891786 1 Acromegaly

Outcome of event

Event ID CASEID OUTC COD
78917869 7891786 OT
78917869 7891786 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
78917869 7891786 Abdominal pain
78917869 7891786 Back pain
78917869 7891786 Bile duct stone
78917869 7891786 Biliary colic
78917869 7891786 Blood pressure systolic increased
78917869 7891786 Cholelithiasis
78917869 7891786 Confusional state
78917869 7891786 Fatigue
78917869 7891786 Loss of consciousness
78917869 7891786 Muscle spasms
78917869 7891786 Pain
78917869 7891786 Sleep disorder
78917869 7891786 Syncope

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
78917869 7891786 1 20071212 0