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
122218682 12221868 2 F 201605 20160703 20160330 20160714 EXP IL-ELI_LILLY_AND_COMPANY-IL201603008108 ELI LILLY AND CO 64.47 YR F Y 0.00000 20160714 CN IL IL

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
122218682 12221868 1 PS FORTEO TERIPARATIDE 1 Subcutaneous 20 UG, QD Y U 21318 20 UG INJECTION QD
122218682 12221868 2 SS FORTEO TERIPARATIDE 1 Subcutaneous 20 UG, QD Y U C520047D 21318 20 UG INJECTION QD
122218682 12221868 3 C CALCIUM CALCIUM 1 U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122218682 12221868 1 Osteoporosis
122218682 12221868 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122218682 12221868 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122218682 12221868 Back pain
122218682 12221868 Blood calcium increased
122218682 12221868 Blood creatinine increased
122218682 12221868 Incorrect drug administration duration
122218682 12221868 Renal disorder

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
122218682 12221868 1 20150611 20160215 0