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
127197281 12719728 1 I 20160507 20160701 20160907 20160907 PER US-JNJFOC-20160702495 JANSSEN 41.85 YR A F Y 65.77000 KG 20160907 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
127197281 12719728 1 SS LEVAQUIN LEVOFLOXACIN 1 Oral 500 MG OR 850 MG N U 0 TABLETS
127197281 12719728 2 PS LEVAQUIN LEVOFLOXACIN 1 Oral 500 MG OR 850 MG N U 20634 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127197281 12719728 1 Middle ear effusion
127197281 12719728 2 Pharyngitis streptococcal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127197281 12719728 Arthralgia
127197281 12719728 Bedridden
127197281 12719728 Fibromyalgia
127197281 12719728 Hypokinesia
127197281 12719728 Pain
127197281 12719728 Paraesthesia
127197281 12719728 Tendon rupture

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
127197281 12719728 1 20160507 20160514 0
127197281 12719728 2 20160507 20160514 0