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
114910182 11491018 2 F 200206 20160720 20150910 20160815 EXP US-JNJFOC-20150810439 JANSSEN 57.10 YR A M Y 99.79000 KG 20160815 CN US US

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
114910182 11491018 1 PS LEVAQUIN LEVOFLOXACIN 1 Oral U U 20634 500 MG TABLETS
114910182 11491018 2 SS LEVAQUIN LEVOFLOXACIN 1 Intravenous (not otherwise specified) 500 MG/100ML U U 20635 INJECTION
114910182 11491018 3 C TYLENOL ACETAMINOPHEN 1 Unknown N 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114910182 11491018 1 Pyrexia
114910182 11491018 2 Product used for unknown indication
114910182 11491018 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114910182 11491018 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114910182 11491018 Musculoskeletal injury
114910182 11491018 Neuropathy peripheral

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
114910182 11491018 1 20020618 0
114910182 11491018 2 20020618 20020628 0
114910182 11491018 3 20020619 0