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
126816461 12681646 1 I 20160416 20160815 20160824 20160824 EXP CN-FRESENIUS KABI-FK201605666 FRESENIUS KABI 36.70 YR F Y 58.00000 KG 20160824 OT CN CN

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
126816461 12681646 1 PS PROPOFOL FRESENIUS (not specified) PROPOFOL 1 Intravenous (not otherwise specified) Y U 10ID1158 19627 120 MG EMULSION FOR INFUSION QD
126816461 12681646 2 SS FENTANYL CITRATE. FENTANYL CITRATE 1 Intravenous (not otherwise specified) 0 .1 MG QD
126816461 12681646 3 SS AZASETRON HYDROCHLORIDE AZASETRON HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0 10 MG QD
126816461 12681646 4 SS CEFUROXIME SODIUM. CEFUROXIME SODIUM 1 Intravenous (not otherwise specified) 0 1.5 G QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126816461 12681646 1 Induction of anaesthesia
126816461 12681646 2 Induction and maintenance of anaesthesia
126816461 12681646 3 Vomiting
126816461 12681646 4 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126816461 12681646 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126816461 12681646 Anaphylactic shock
126816461 12681646 Cardiac arrest
126816461 12681646 Laryngeal oedema

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
126816461 12681646 1 20160416 20160416 0
126816461 12681646 2 20160416 20160416 0
126816461 12681646 3 20160416 20160416 0
126816461 12681646 4 20160416 20160416 0