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
125212481 12521248 1 I 20151222 20160622 20160701 20160701 EXP CN-BAXTER-2016BAX033682 BAXTER 79.00 YR F Y 40.00000 KG 20160701 MD 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
125212481 12521248 1 PS 0.9% SODIUM CHLORIDE INJECTION SODIUM CHLORIDE 1 Intravenous drip Y S1509033 16677 100 ML INJECTION QD
125212481 12521248 2 SS SULPERAZONE CEFOPERAZONE SODIUMSULBACTAM SODIUM 1 Intravenous drip Y M34151 16677 3 G POWDER FOR INJECTION QD
125212481 12521248 3 SS METOCLOPRAMIDE HYDROCHLORIDE. METOCLOPRAMIDE HYDROCHLORIDE 1 Intramuscular U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125212481 12521248 1 Medication dilution
125212481 12521248 2 Lung infection
125212481 12521248 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125212481 12521248 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125212481 12521248 Abdominal distension
125212481 12521248 Abdominal pain
125212481 12521248 Chest discomfort
125212481 12521248 Depressed mood
125212481 12521248 Diarrhoea
125212481 12521248 Nausea
125212481 12521248 Oedema peripheral
125212481 12521248 Wheezing

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
125212481 12521248 1 20151222 20151222 0
125212481 12521248 2 20151222 20151222 0
125212481 12521248 3 20151222 0