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
123204352 12320435 2 F 201603 20160830 20160429 20160913 EXP TH-ELI_LILLY_AND_COMPANY-TH201603002416 ELI LILLY AND CO 84.00 YR F Y 0.00000 20160909 CN TH TH

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
123204352 12320435 1 PS FORTEO TERIPARATIDE 1 Subcutaneous 20 UG, QD Y 21318 20 UG INJECTION QD
123204352 12320435 2 C GABAPENTIN. GABAPENTIN 1 100 MG, UNK U 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123204352 12320435 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
123204352 12320435 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123204352 12320435 Abdominal discomfort
123204352 12320435 Abdominal pain
123204352 12320435 Back pain
123204352 12320435 Constipation
123204352 12320435 Dizziness
123204352 12320435 Dysuria
123204352 12320435 Erythema
123204352 12320435 Hypoaesthesia
123204352 12320435 Injection site pain
123204352 12320435 Urinary tract infection

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
123204352 12320435 1 20160122 201603 0