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
126474981 12647498 1 I 2012 0 20160811 20160811 DIR 0.00 F N 125.00000 LBS 20160807 N 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
126474981 12647498 1 PS ACTONEL RISEDRONATE SODIUM 1 Oral 1 TABLET N 0 35 MG COATED TABLET QW
126474981 12647498 3 C TRIAMTERENE HCTZ HYDROCHLOROTHIAZIDETRIAMTERENE 1 0
126474981 12647498 5 C CALCIUM CALCIUM 1 0
126474981 12647498 7 C VITAMIN D3 CHOLECALCIFEROL 1 0
126474981 12647498 9 C VITAMIN B12 CYANOCOBALAMIN 1 0
126474981 12647498 11 C MULTI VITAMIN VITAMINS 1 0
126474981 12647498 13 C AREDS 2 MINERALSVITAMINS 1 0
126474981 12647498 15 C ASPIRIN. ASPIRIN 1 0
126474981 12647498 17 C MAGNESIUM MAGNESIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126474981 12647498 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126474981 12647498 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126474981 12647498 Arthralgia
126474981 12647498 Chills
126474981 12647498 Fatigue
126474981 12647498 Hyperhidrosis
126474981 12647498 Influenza
126474981 12647498 Middle insomnia
126474981 12647498 Musculoskeletal disorder
126474981 12647498 Myalgia
126474981 12647498 Nasopharyngitis

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
126474981 12647498 1 201102 20140929 0