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
125206921 12520692 1 I 201606 20160615 20160701 20160701 PER US-ELI_LILLY_AND_COMPANY-US201606006207 ELI LILLY AND CO 0.00 F Y 0.00000 20160701 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
125206921 12520692 1 PS FORTEO TERIPARATIDE 1 Unknown UNK, QD C471303D 21318 INJECTION QD
125206921 12520692 2 C RAMIPRIL. RAMIPRIL 1 U 0
125206921 12520692 3 C SIMVASTATIN. SIMVASTATIN 1 U 0
125206921 12520692 4 C MELOXICAM. MELOXICAM 1 U 0
125206921 12520692 5 C CALCIUM CALCIUM 1 U 0
125206921 12520692 6 C OMEPRAZOLE. OMEPRAZOLE 1 20 MG, UNK U 0 20 MG
125206921 12520692 7 C ASPIRIN /00002701/ ASPIRIN 1 U 0
125206921 12520692 8 C FAMOTIDINE. FAMOTIDINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125206921 12520692 1 Bone disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125206921 12520692 Abdominal distension
125206921 12520692 Abdominal pain upper
125206921 12520692 Asthenia
125206921 12520692 Chest discomfort
125206921 12520692 Drug dose omission
125206921 12520692 Dyspnoea
125206921 12520692 Lethargy
125206921 12520692 Muscular weakness
125206921 12520692 Nausea
125206921 12520692 Vomiting

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
125206921 12520692 1 20160609 0