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
127011041 12701104 1 I 20160720 0 20160830 20160830 DIR 57.00 YR F N 160.00000 LBS 20160829 N COUNTRY NOT SPECIFIED

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
127011041 12701104 1 PS RECLAST ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) ONCE A YEAR INTO A VEIN N D 0
127011041 12701104 3 C STATIN UNSPECIFIED INGREDIENT 1 0
127011041 12701104 5 C THYROID MEDICATION UNSPECIFIED INGREDIENT 1 0
127011041 12701104 7 C METHOTREXATE. METHOTREXATE 1 0
127011041 12701104 9 C TYLENOL ACETAMINOPHEN 1 0
127011041 12701104 11 C VITAMN B12 2 0
127011041 12701104 13 C VITAMIN D3 CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127011041 12701104 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127011041 12701104 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127011041 12701104 Alopecia
127011041 12701104 Chest pain
127011041 12701104 Dyspnoea
127011041 12701104 Nausea
127011041 12701104 Pruritus generalised
127011041 12701104 Rash

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
127011041 12701104 1 20160720 0