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
127992081 12799208 1 I 20160131 20160920 20160930 20160930 EXP GB-HORIZON-PRE-0275-2016 HORIZON 0.00 F Y 0.00000 20160930 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
127992081 12799208 1 PS PREDNISONE. PREDNISONE 1 U 202020
127992081 12799208 2 SS Clarithromycin Sandoz CLARITHROMYCIN 1 Oral 1 G DAILY U 0 1 G
127992081 12799208 3 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 0 500 MG
127992081 12799208 4 C Paracetamol ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127992081 12799208 1 Product used for unknown indication
127992081 12799208 2 Lower respiratory tract infection
127992081 12799208 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127992081 12799208 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127992081 12799208 Abdominal pain
127992081 12799208 Diarrhoea
127992081 12799208 Dyskinesia
127992081 12799208 Dyspnoea
127992081 12799208 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
127992081 12799208 2 201509 0