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
126907921 12690792 1 I 20150123 20160816 20160826 20160826 EXP NO-NOMAADVRE-NOMAADVRE-2016-22445 NO-TEVA-686744ACC TEVA 57.00 YR M Y 0.00000 20160826 MD 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
126907921 12690792 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 1000 MILLIGRAM DAILY; N 74124 500 MG TABLET BID
126907921 12690792 2 SS FLAGYL METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE 1 Oral 1200 MILLIGRAM DAILY; U 0 400 MG TABLET TID
126907921 12690792 3 C Panodil forte 2 Oral 0 TABLET
126907921 12690792 4 C AMLODIPIN SANDOZ 2 0 10 MG
126907921 12690792 5 C LIPITOR ATORVASTATIN CALCIUM 1 0 40 MG
126907921 12690792 6 C IBUPROFEN. IBUPROFEN 1 Cutaneous 0 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126907921 12690792 1 Prophylaxis
126907921 12690792 2 Prophylaxis
126907921 12690792 4 Hypertension
126907921 12690792 5 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
126907921 12690792 OT
126907921 12690792 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126907921 12690792 Depression
126907921 12690792 Feeling hot
126907921 12690792 Gait disturbance
126907921 12690792 Osteonecrosis
126907921 12690792 Swelling

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
126907921 12690792 1 20150115 20150122 0
126907921 12690792 2 20150115 20150122 0