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
125779881 12577988 1 I 201605 20160705 20160721 20160721 PER US-ELI_LILLY_AND_COMPANY-US201607002876 ELI LILLY AND CO 78.71 YR F Y 0.00000 20160721 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
125779881 12577988 1 PS FORTEO TERIPARATIDE 1 Unknown 20 MG, UNKNOWN 21318 20 MG INJECTION
125779881 12577988 2 SS FORTEO TERIPARATIDE 1 Unknown 20 UG, UNKNOWN C465010C 21318 20 UG INJECTION
125779881 12577988 3 C LIPITOR ATORVASTATIN CALCIUM 1 10 MG, UNK U 0 10 MG
125779881 12577988 4 C ZANTAC RANITIDINE HYDROCHLORIDE 1 150 MG, UNK U 0 150 MG
125779881 12577988 5 C DEXILANT DEXLANSOPRAZOLE 1 60 MG, UNK U 0 60 MG
125779881 12577988 6 C MYLANTA ALUMINUM HYDROXIDEDIMETHICONEMAGNESIUM HYDROXIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125779881 12577988 1 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125779881 12577988 Blood calcium increased
125779881 12577988 Nausea
125779881 12577988 Palpitations
125779881 12577988 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
125779881 12577988 1 201508 0