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
127877561 12787756 1 I 20160131 20160920 20160928 20160928 EXP GB-GLAXOSMITHKLINE-GB2016137517 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160928 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
127877561 12787756 1 SS PREDNISONE. PREDNISONE 1 Unknown UNK U 0
127877561 12787756 2 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 500 MG, UNK U 21077 500 MG
127877561 12787756 3 SS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral 1 G, QD U 0 1 G QD
127877561 12787756 4 C Paracetamol ACETAMINOPHEN 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127877561 12787756 1 Product used for unknown indication
127877561 12787756 2 Product used for unknown indication
127877561 12787756 3 Lower respiratory tract infection
127877561 12787756 4 Arthralgia

Outcome of event

Event ID CASEID OUTC COD
127877561 12787756 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127877561 12787756 Abdominal pain
127877561 12787756 Diarrhoea
127877561 12787756 Dyskinesia
127877561 12787756 Dyspnoea
127877561 12787756 White blood cell count decreased

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
127877561 12787756 3 201509 0