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
127404271 12740427 1 I 20160224 20160303 20160913 20160913 EXP AU-ELI_LILLY_AND_COMPANY-AU201603001950 ELI LILLY AND CO 52.54 YR F Y 0.00000 20160912 CN AU AU

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
127404271 12740427 1 PS FORTEO TERIPARATIDE 1 Subcutaneous UNK, QD 21318 20 UG INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127404271 12740427 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127404271 12740427 HO
127404271 12740427 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127404271 12740427 Bone pain
127404271 12740427 Depressed mood
127404271 12740427 Fall
127404271 12740427 Headache
127404271 12740427 Hypotension
127404271 12740427 Influenza like illness
127404271 12740427 Injection site pain
127404271 12740427 Joint injury
127404271 12740427 Muscle spasms
127404271 12740427 Nausea
127404271 12740427 Osteonecrosis
127404271 12740427 Pain
127404271 12740427 Vitamin D 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
127404271 12740427 1 20160224 0