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
126089001 12608900 1 I 2016 20160623 20160730 20160730 EXP PL-AMGEN-POLSP2016082641 AMGEN 79.00 YR E F Y 0.00000 20160730 CN PL PL

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
126089001 12608900 1 PS PROLIA DENOSUMAB 1 Unknown UNK U 125320 SOLUTION FOR INJECTION
126089001 12608900 2 C FOSTEX 2 UNK 0
126089001 12608900 3 C CALPEROS CALCIUM CARBONATE 1 1000 MG, UNK 0 1000 MG
126089001 12608900 4 C DEFLEGMIN 2 UNK 0
126089001 12608900 5 C ACARD ASPIRIN 1 UNK 0
126089001 12608900 6 C PREDUCTAL TRIMETAZIDINE DIHYDROCHLORIDE 1 UNK 0
126089001 12608900 7 C VITAMIN K PHYTONADIONE 1 UNK 0
126089001 12608900 8 C VITAMIN D CHOLECALCIFEROL 1 2000 IU, UNK 0 2000 IU

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126089001 12608900 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126089001 12608900 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126089001 12608900 Adverse event
126089001 12608900 Arthralgia
126089001 12608900 Asthma
126089001 12608900 Bone pain
126089001 12608900 Rash pruritic
126089001 12608900 Sensory disturbance
126089001 12608900 Sensory loss
126089001 12608900 Toothache
126089001 12608900 Urinary incontinence

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
126089001 12608900 1 20160531 0