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
123009082 12300908 2 F 20150123 20160816 20160425 20160826 EXP NO-BAYER-2016-070618 BAYER 57.00 YR A M Y 0.00000 20160826 LW NO NO

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
123009082 12300908 1 PS Ciproxin 500 mg filmcoated tablets CIPROFLOXACIN 1 Oral 500 MG, BID N UNK 19537 500 MG TABLET BID
123009082 12300908 2 SS FLAGYL METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE 1 Oral 400 MG, TID UNK 0 400 MG TID
123009082 12300908 3 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown 40 MG, UNK 0 40 MG
123009082 12300908 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 10 MG, UNK 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123009082 12300908 1 Prophylaxis
123009082 12300908 2 Prophylaxis
123009082 12300908 3 Hypercholesterolaemia
123009082 12300908 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
123009082 12300908 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
123009082 12300908 Arthralgia
123009082 12300908 Arthritis
123009082 12300908 Depression
123009082 12300908 Feeling hot
123009082 12300908 Gait disturbance
123009082 12300908 Joint swelling
123009082 12300908 Osteonecrosis

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
123009082 12300908 1 20150115 20150121 0
123009082 12300908 2 20150115 20150121 0