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
125308901 12530890 1 I 20160430 20160701 20160706 20160706 EXP GXKR2016DE003074 SANDOZ 0.00 Y 0.00000 20160706 OT DE DE

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
125308901 12530890 1 PS ALLOPURINOL. ALLOPURINOL 1 Oral 150 MG, UNK Y 70269 150 MG
125308901 12530890 2 C DAFIRO AMLODIPINEVALSARTAN 1 Oral 0
125308901 12530890 3 C BISPROLOL COMP 2 Oral 0
125308901 12530890 4 C MARCUMAR PHENPROCOUMON 1 Oral ACCORDING TO INR 0
125308901 12530890 5 C LEXOTANIL BROMAZEPAM 1 Oral AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125308901 12530890 1 Hyperuricaemia
125308901 12530890 2 Product used for unknown indication
125308901 12530890 3 Product used for unknown indication
125308901 12530890 4 Product used for unknown indication
125308901 12530890 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125308901 12530890 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125308901 12530890 Blister
125308901 12530890 General physical health deterioration
125308901 12530890 Nausea
125308901 12530890 Pain
125308901 12530890 Toxic epidermal necrolysis

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
125308901 12530890 1 20160422 20160510 0
125308901 12530890 2 2011 0
125308901 12530890 3 2011 0
125308901 12530890 4 2011 0
125308901 12530890 5 2011 0