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
116017643 11601764 3 F 201501 20160627 20151006 20160701 EXP US-AMGEN-USASP2015045837 AMGEN 74.00 YR E M 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
116017643 11601764 1 PS PROLIA DENOSUMAB 1 Unknown UNK UNK, Q6MO N 1053088 125320 SOLUTION FOR INJECTION
116017643 11601764 2 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 UNK 0
116017643 11601764 3 C HYDROCODONE HYDROCODONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116017643 11601764 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
116017643 11601764 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116017643 11601764 Arthralgia
116017643 11601764 Back pain
116017643 11601764 Chronic obstructive pulmonary disease
116017643 11601764 Injection site discomfort
116017643 11601764 Injection site pain
116017643 11601764 Musculoskeletal pain
116017643 11601764 Peripheral swelling

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
116017643 11601764 1 201501 0