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
110220283 11022028 3 F 201604 20160721 20150413 20160802 EXP US-ELI_LILLY_AND_COMPANY-US201503010359 ELI LILLY AND CO 81.54 YR F Y 0.00000 20160802 CN US US

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
110220283 11022028 1 PS FORTEO TERIPARATIDE 1 Unknown UNK UNK, UNKNOWN 21318 INJECTION
110220283 11022028 2 SS FORTEO TERIPARATIDE 1 Unknown UNK UNK, UNKNOWN 21318 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110220283 11022028 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
110220283 11022028 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110220283 11022028 Decreased appetite
110220283 11022028 Fall
110220283 11022028 Flatulence
110220283 11022028 Gastrooesophageal reflux disease
110220283 11022028 Haemorrhage
110220283 11022028 Head injury
110220283 11022028 Memory impairment
110220283 11022028 Tinnitus
110220283 11022028 Tooth disorder
110220283 11022028 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
110220283 11022028 1 201404 0