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
127498421 12749842 1 I 20160912 20160916 20160916 EXP JP-GLAXOSMITHKLINE-JP2016JPN133171 GLAXOSMITHKLINE 28.00 YR F Y 0.00000 20160916 CN JP JP

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
127498421 12749842 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) UNK U 21077 INHALATION POWDER
127498421 12749842 2 SS PROCATEROL PROCATEROL HYDROCHLORIDE 1 Respiratory (inhalation) U 0
127498421 12749842 3 SS FLOMOXEF SODIUM FLOMOXEF SODIUM 1 Intravenous (not otherwise specified) 1 G, U U 0 1 G
127498421 12749842 4 SS BUPIVACAINE HYDROCHLORIDE HYDRATE BUPIVACAINE HYDROCHLORIDE 1 Other 2.4 ML, U U 0 2.4 ML
127498421 12749842 5 SS FENTANYL. FENTANYL 1 Other 0.01 MG, U U 0 .01 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127498421 12749842 1 Asthma
127498421 12749842 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
127498421 12749842 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127498421 12749842 Anaphylactic shock
127498421 12749842 Dyspnoea
127498421 12749842 Exposure during pregnancy
127498421 12749842 Face oedema
127498421 12749842 Lip oedema
127498421 12749842 Nausea
127498421 12749842 Premature labour
127498421 12749842 Stridor
127498421 12749842 Tracheal stenosis
127498421 12749842 Urticaria
127498421 12749842 Wheezing

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found