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
79351324 7935132 4 F 20160803 20110509 20160811 EXP US-ASTRAZENECA-2011SE25157 ASTRAZENECA 55.00 YR F Y 0.00000 20160811 CN US US

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
79351324 7935132 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN 21153 40 MG CAPSULE
79351324 7935132 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN 21153 40 MG TABLET QD
79351324 7935132 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 10.0MG UNKNOWN 0 10 MG TABLET
79351324 7935132 4 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 40.0MG UNKNOWN 0 40 MG TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
79351324 7935132 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
79351324 7935132 Activities of daily living impaired
79351324 7935132 Blindness
79351324 7935132 Drug dose omission
79351324 7935132 Immune system disorder
79351324 7935132 Malaise
79351324 7935132 Neoplasm malignant
79351324 7935132 Ulcer
79351324 7935132 Vomiting

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

no results found

Therapies reported

no results found