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
110955977 11095597 7 F 2012 20160817 20150506 20160824 EXP PHHY2015BR053980 NOVARTIS 0.00 M Y 84.00000 KG 20160824 MD BR BR

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
110955977 11095597 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO 21008 30 MG SUSPENSION /month
110955977 11095597 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO 21008 30 MG SUSPENSION /month
110955977 11095597 3 C SIMVASTATIN. SIMVASTATIN 1 Oral 5 DF OF 30 MG, QD 0 5 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110955977 11095597 1 Acromegaly
110955977 11095597 3 Head discomfort

Outcome of event

Event ID CASEID OUTC COD
110955977 11095597 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110955977 11095597 Asthenia
110955977 11095597 Blindness transient
110955977 11095597 Confusional state
110955977 11095597 Diabetes mellitus
110955977 11095597 Ear discomfort
110955977 11095597 Eye colour change
110955977 11095597 Eye pain
110955977 11095597 Headache
110955977 11095597 Hypertension
110955977 11095597 Hyperthyroidism
110955977 11095597 Hypoacusis
110955977 11095597 Influenza
110955977 11095597 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
110955977 11095597 1 2012 2015 0
110955977 11095597 2 201504 0
110955977 11095597 3 201504 0