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
127975531 12797553 1 I 20160921 20160930 20160930 EXP US-AMGEN-USASP2016129615 AMGEN 0.00 F Y 0.00000 20160929 OT 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
127975531 12797553 1 PS PROLIA DENOSUMAB 1 Unknown UNK U 125320 SOLUTION FOR INJECTION
127975531 12797553 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, QD 0 20 MG QD
127975531 12797553 3 SS LYRICA PREGABALIN 1 Oral 75 MG, BID 0 75 MG BID
127975531 12797553 4 C METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 Oral 25 MG, QD 0 25 MG QD
127975531 12797553 5 C FELODIPINE. FELODIPINE 1 Oral 10 MG, QD 0 10 MG QD
127975531 12797553 6 C FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QWK 0 70 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127975531 12797553 1 Osteoporosis postmenopausal
127975531 12797553 2 Product used for unknown indication
127975531 12797553 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127975531 12797553 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127975531 12797553 Arthralgia
127975531 12797553 Back pain
127975531 12797553 Headache
127975531 12797553 Lumbar spinal stenosis
127975531 12797553 Macular degeneration
127975531 12797553 Pain in extremity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found