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
127726162 12772616 2 F 20160819 20160919 20160922 20160924 EXP PHHY2016FR130020 SANDOZ 42.00 YR M Y 0.00000 20160924 OT FR FR

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
127726162 12772616 1 SS TEGRETOL CARBAMAZEPINE 1 Oral 400 MG, BID 0 400 MG BID
127726162 12772616 2 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Intravenous (not otherwise specified) UNK 96000 MG Y 76593
127726162 12772616 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, BID 96000 MG Y 76593 500 MG BID
127726162 12772616 4 SS DILANTIN PHENYTOIN 1 Oral 50 MG, BID 0 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127726162 12772616 1 Epilepsy
127726162 12772616 2 Cystitis
127726162 12772616 4 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127726162 12772616 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127726162 12772616 Condition aggravated
127726162 12772616 Leukopenia
127726162 12772616 Thrombocytopenia

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
127726162 12772616 2 20160506 20160516 0
127726162 12772616 3 20160516 20160819 0