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
127644451 12764445 1 I 20160908 20160920 20160920 EXP IT-MINISAL02-373760 IT-TEVA-693067ACC TEVA 12.00 YR M Y 0.00000 20160921 MD 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
127644451 12764445 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral 500 MG DAILY Y 76361 500 MG
127644451 12764445 2 SS OXACILLIN OXACILLIN SODIUM 1 Oral DAILY Y 0
127644451 12764445 3 SS Trimethoprim + Sulfamethoxazole SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 800 MG/KG DAILY Y 0 800 MG/KG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127644451 12764445 1 Bone abscess
127644451 12764445 2 Bone abscess
127644451 12764445 3 Bone abscess

Outcome of event

Event ID CASEID OUTC COD
127644451 12764445 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127644451 12764445 Aphthous ulcer
127644451 12764445 Arthralgia
127644451 12764445 Headache
127644451 12764445 Pyrexia
127644451 12764445 Rash
127644451 12764445 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
127644451 12764445 1 20160708 20160727 0
127644451 12764445 2 20160708 20160727 0
127644451 12764445 3 20160811 20160824 0