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
127534471 12753447 1 I 20160907 20160915 20160915 EXP PHHY2016IT124458 SANDOZ 12.00 YR M Y 0.00000 20160915 OT IT IT

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
127534471 12753447 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral 500 MG, QD 77438 500 MG QD
127534471 12753447 2 SS OXACILLIN OXACILLIN SODIUM 1 Oral 1 G/KG, QD Y U 0 QD
127534471 12753447 3 SS SULFAMETOXAZOL/TRIMETOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 800 MG/KG, QD Y U 0 800 MG/KG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127534471 12753447 1 Bone abscess
127534471 12753447 2 Bone abscess
127534471 12753447 3 Bone abscess

Outcome of event

Event ID CASEID OUTC COD
127534471 12753447 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127534471 12753447 Aphthous ulcer
127534471 12753447 Arthralgia
127534471 12753447 Headache
127534471 12753447 Leukopenia
127534471 12753447 Pyrexia
127534471 12753447 Rash
127534471 12753447 Thrombocytopenia
127534471 12753447 Vomiting

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
127534471 12753447 1 20160708 20160727 0
127534471 12753447 2 20160708 20160727 0
127534471 12753447 3 20160811 20160824 0