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
127598791 12759879 1 I 201607 20160908 20160919 20160919 EXP IT-MINISAL02-373760 IT-MYLANLABS-2016M1038966 MYLAN 0.00 Y 0.00000 20160919 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
127598791 12759879 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral 500 MG, QD Y U 76276 500 MG QD
127598791 12759879 2 SS OXACILLIN OXACILLIN SODIUM 1 Oral UNK UNK, QD Y 0 QD
127598791 12759879 3 SS SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 800 MG/KG, QD Y 0 800 MG/KG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127598791 12759879 1 Bone abscess
127598791 12759879 2 Bone abscess
127598791 12759879 3 Bone abscess

Outcome of event

Event ID CASEID OUTC COD
127598791 12759879 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127598791 12759879 Aphthous ulcer
127598791 12759879 Arthralgia
127598791 12759879 Headache
127598791 12759879 Leukopenia
127598791 12759879 Neutropenia
127598791 12759879 Pyrexia
127598791 12759879 Rash
127598791 12759879 Thrombocytopenia
127598791 12759879 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
127598791 12759879 1 20160708 20160727 0
127598791 12759879 2 20160708 20160727 0
127598791 12759879 3 20160811 20160824 0