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
126774011 12677401 1 I 20160816 20160823 20160823 EXP CA-ELI_LILLY_AND_COMPANY-CA201608008844 ELI LILLY AND CO 74.00 YR F Y 66.00000 KG 20160822 CN CA CA

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
126774011 12677401 1 PS FORTEO TERIPARATIDE 1 Subcutaneous 20 UG, QD U U 21318 20 UG INJECTION QD
126774011 12677401 2 C AMITRIPTYLINE AMITRIPTYLINE 1 U 0 TABLET
126774011 12677401 3 C ASPIRIN /00002701/ ASPIRIN 1 U 0
126774011 12677401 4 C ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 U 0 TABLET
126774011 12677401 5 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 U 0
126774011 12677401 6 C CHOLECALCIFEROL CHOLECALCIFEROL 1 U 0
126774011 12677401 7 C DILTIAZEM. DILTIAZEM 1 U 0
126774011 12677401 8 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 U 0 TABLET
126774011 12677401 9 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126774011 12677401 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126774011 12677401 HO
126774011 12677401 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126774011 12677401 Balance disorder
126774011 12677401 Confusional state
126774011 12677401 Disorientation
126774011 12677401 Fall
126774011 12677401 Headache
126774011 12677401 Hypercalcaemia
126774011 12677401 Intracranial aneurysm
126774011 12677401 Memory impairment
126774011 12677401 Presyncope

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found