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
73386762 7338676 2 F 20160801 20100331 20160808 EXP DE-ASTRAZENECA-2010SE12647 ASTRAZENECA 75.00 YR M Y 0.00000 20160808 OT DE DE

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
73386762 7338676 1 PS ESOMEPRAZOLE ESOMEPRAZOLE 1 Intravenous (not otherwise specified) 40-80 MG/DAY Y U 21689 INJECTION
73386762 7338676 2 C INSULIN INSULIN NOS 1 0
73386762 7338676 3 C HEPARIN HEPARIN SODIUM 1 800 IU/H 0
73386762 7338676 4 C FUROSEMIDE. FUROSEMIDE 1 40-120 MG/DAY 0
73386762 7338676 5 C AMIODARONE AMIODARONE 1 0
73386762 7338676 6 C MEROPENEM. MEROPENEM 1 0
73386762 7338676 7 C LINEZOLID. LINEZOLID 1 0
73386762 7338676 8 C PROPOFOL. PROPOFOL 1 0
73386762 7338676 9 C SUFENTANIL SUFENTANIL 1 0
73386762 7338676 10 C CATECHOLAMINES UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73386762 7338676 1 Prophylaxis against gastrointestinal ulcer
73386762 7338676 8 Sedation
73386762 7338676 9 Sedation

Outcome of event

Event ID CASEID OUTC COD
73386762 7338676 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
73386762 7338676 Rhabdomyolysis

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

no results found

Therapies reported

no results found