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
125921471 12592147 1 I 20160520 20160715 20160726 20160726 EXP GB-MHRA-EYC 00142336 GB-DRREDDYS-GER/UKI/16/0081596 DR REDDYS 74.00 YR M Y 71.66000 KG 20160726 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
125921471 12592147 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 10500 MG N U UNKNOWN 75593 750 MG BID
125921471 12592147 2 C DICLOFLEX 2 0 75 MG QD
125921471 12592147 3 C ELIQUIS APIXABAN 1 0 2.5 MG BID
125921471 12592147 4 C OMEPRAZOLE. OMEPRAZOLE 1 0 20 MG QD
125921471 12592147 5 C TAMSULOSIN TAMSULOSIN 1 0 400 UG MODIFIED-RELEASE CAPSULE, HARD QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125921471 12592147 1 Lung infection
125921471 12592147 2 Product used for unknown indication
125921471 12592147 3 Product used for unknown indication
125921471 12592147 4 Product used for unknown indication
125921471 12592147 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125921471 12592147 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125921471 12592147 Pain
125921471 12592147 Peripheral swelling
125921471 12592147 Swelling face

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
125921471 12592147 1 20160513 20160524 0