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
125549141 12554914 1 I 20130108 20160325 20160713 20160713 PER US-ASTRAZENECA-2016SE33787 ASTRAZENECA 14259.00 DY F Y 0.00000 20160714 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
125549141 12554914 1 PS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 19810 CAPSULE
125549141 12554914 2 SS SEROQUEL QUETIAPINE FUMARATE 1 Oral U 0 TABLET
125549141 12554914 3 SS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown U 0
125549141 12554914 4 SS LYRICA PREGABALIN 1 Oral U 0 1 DF CAPSULE BID
125549141 12554914 5 SS DAYPRO OXAPROZIN 1 Unknown U 0
125549141 12554914 6 SS PROTONIX PANTOPRAZOLE SODIUM 1 Unknown U 0
125549141 12554914 7 SS LEVOXYL LEVOTHYROXINE SODIUM 1 Unknown U 0
125549141 12554914 8 SS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Unknown U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125549141 12554914 Dizziness
125549141 12554914 Drug hypersensitivity
125549141 12554914 Drug ineffective
125549141 12554914 Feeling abnormal

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
125549141 12554914 4 20160217 0