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
125279501 12527950 1 I 201601 20160628 20160705 20160705 EXP CA-AMGEN-CANSL2016084068 AMGEN 67.00 YR E F Y 0.00000 20160705 MD 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
125279501 12527950 1 PS PROLIA DENOSUMAB 1 Unknown UNK 125320 SOLUTION FOR INJECTION
125279501 12527950 2 C TELMISARTAN. TELMISARTAN 1 0
125279501 12527950 3 C ATORVASTATIN ATORVASTATIN 1 0
125279501 12527950 4 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
125279501 12527950 5 C LORAZEPAM. LORAZEPAM 1 HS, AS NECESSARY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125279501 12527950 1 Osteoporosis
125279501 12527950 5 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
125279501 12527950 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125279501 12527950 Arthritis
125279501 12527950 Chest pain
125279501 12527950 Diabetes mellitus
125279501 12527950 Muscle spasms
125279501 12527950 Pyrexia
125279501 12527950 Urinary tract infection
125279501 12527950 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
125279501 12527950 1 20150621 0