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
85357129 8535712 9 F 20160219 20160811 20120430 20160816 EXP PHHY2012CA034520 NOVARTIS 63.52 YR F Y 0.00000 20160816 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
85357129 8535712 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, QMO U 21008 40 MG SUSPENSION /month
85357129 8535712 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 20 MG, QMO (EVERY 4 WEEKS) U 21008 20 MG SUSPENSION /month
85357129 8535712 3 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Unknown UNK U 21008 SUSPENSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
85357129 8535712 1 Acromegaly

Outcome of event

Event ID CASEID OUTC COD
85357129 8535712 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
85357129 8535712 Blood pressure diastolic increased
85357129 8535712 Blood pressure increased
85357129 8535712 Cough
85357129 8535712 Drug ineffective
85357129 8535712 Dysphonia
85357129 8535712 Fatigue
85357129 8535712 Head discomfort
85357129 8535712 Hyperhidrosis
85357129 8535712 Labyrinthitis
85357129 8535712 Mass
85357129 8535712 Nausea
85357129 8535712 Needle issue
85357129 8535712 Productive cough
85357129 8535712 Vertigo
85357129 8535712 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
85357129 8535712 1 20100709 0
85357129 8535712 2 20120718 0
85357129 8535712 3 20160420 0