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
126577631 12657763 1 I 20160719 20160810 20160816 20160816 EXP GB-MHRA-MIDB-DEE84EEB-EBFB-4133-9F74-BF4666516B9C PHHY2016GB109687 SANDOZ 13.00 YR F Y 0.00000 20160816 OT 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
126577631 12657763 1 PS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Oral 225 MG, QID 13500 MG Y 64159 225 MG SOLUTION QID
126577631 12657763 2 C CHLORPHENAMINE CHLORPHENIRAMINE MALEATE 1 Oral 4 MG U 0 4 MG
126577631 12657763 3 C FLUCLOXACILLIN FLUCLOXACILLIN 1 Intravenous drip 1900 MG, QID 167200 MG Y 0 1900 MG QID
126577631 12657763 4 C PARACETAMOL ACETAMINOPHEN 1 Oral 570 MG, QID U 0 570 MG QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126577631 12657763 1 Bone tuberculosis
126577631 12657763 2 Product used for unknown indication
126577631 12657763 3 Product used for unknown indication
126577631 12657763 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126577631 12657763 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126577631 12657763 Pruritus
126577631 12657763 Rash generalised

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
126577631 12657763 1 20160704 0
126577631 12657763 3 20160627 0