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
126824431 12682443 1 I 201410 20160822 20160825 20160825 PER US-ELI_LILLY_AND_COMPANY-US201608011206 ELI LILLY AND CO 0.00 F Y 0.00000 20160825 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
126824431 12682443 1 PS FORTEO TERIPARATIDE 1 Unknown UNK, QD 21318 INJECTION QD
126824431 12682443 2 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 U 0
126824431 12682443 3 C FLUDROCORTISONE FLUDROCORTISONE 1 U 0
126824431 12682443 4 C OXYBUTON /00054001/ 2 U 0
126824431 12682443 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 U 0
126824431 12682443 6 C AMLODIPIN /00972401/ AMLODIPINE BESYLATE 1 U 0
126824431 12682443 7 C CALCIUM CALCIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126824431 12682443 1 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126824431 12682443 Dizziness
126824431 12682443 Fatigue
126824431 12682443 Muscular weakness

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
126824431 12682443 1 201410 0