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
125818011 12581801 1 I 20160514 20160714 20160722 20160722 EXP GB-MHRA-EYC 00142252 GB-DRREDDYS-GER/UKI/16/0081579 DR REDDYS 51.00 YR F Y 56.00000 KG 20160722 MD 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
125818011 12581801 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 1500 MG N U UNKNOWN 75593 750 MG BID
125818011 12581801 2 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
125818011 12581801 3 C MELOXICAM. MELOXICAM 1 0
125818011 12581801 4 C PREGABALIN. PREGABALIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125818011 12581801 1 Pseudomonas infection
125818011 12581801 2 Product used for unknown indication
125818011 12581801 3 Product used for unknown indication
125818011 12581801 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125818011 12581801 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125818011 12581801 Abasia
125818011 12581801 Musculoskeletal pain
125818011 12581801 Neuralgia
125818011 12581801 Tendonitis

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
125818011 12581801 1 20160513 20160515 0