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
125728081 12572808 1 I 20160630 20160711 20160720 20160720 EXP HN-BAXTER-2016BAX037575 BAXTER 61.00 YR F Y 0.00000 20160720 MD HN HN

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
125728081 12572808 1 PS LACTATED RINGERS CALCIUM CHLORIDEPOTASSIUM CHLORIDESODIUM CHLORIDESODIUM LACTATE 1 Intravenous (not otherwise specified) Y V16D06K2 16682 500 ML SOLUTION FOR INJECTION
125728081 12572808 2 SS SODIUM CHLORIDE. SODIUM CHLORIDE 1 Intravenous (not otherwise specified) U 0
125728081 12572808 3 SS RILATEN ROCIVERINE 1 Intravenous (not otherwise specified) U 0
125728081 12572808 4 SS BETA DUO BETAMETHASONE 1 Intravenous (not otherwise specified) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125728081 12572808 1 Fluid replacement
125728081 12572808 2 Medication dilution
125728081 12572808 3 Gastrointestinal pain
125728081 12572808 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125728081 12572808 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125728081 12572808 Headache
125728081 12572808 Somnolence
125728081 12572808 Tremor

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
125728081 12572808 1 20160630 20160630 0
125728081 12572808 2 20160630 20160630 0
125728081 12572808 3 20160630 20160630 0
125728081 12572808 4 20160630 20160630 0