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
126595821 12659582 1 I 20120911 20120924 20160817 20160817 EXP GB-PFIZER INC-2012235960 PFIZER 0.00 M Y 80.00000 KG 20160817 CN GB GB

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
126595821 12659582 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, UNK U 77245

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126595821 12659582 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126595821 12659582 Arthralgia
126595821 12659582 Arthropathy
126595821 12659582 Joint dislocation
126595821 12659582 Pain in extremity
126595821 12659582 Tendon pain

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
126595821 12659582 1 20120903 20120910 0