The Safety Rates Drug Report

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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
127062801 12706280 1 I 2005 20160602 20160901 20160901 PER US-ASTRAZENECA-2016SE59719 ASTRAZENECA 847.00 MON F Y 63.50000 KG 20160901 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
127062801 12706280 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40.0MG UNKNOWN UNKNOWN 21153 40 MG
127062801 12706280 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, 2 PUFFS TWICE A DAY U UNKNOWN 0
127062801 12706280 3 SS METOPROLOL. METOPROLOL 1 Oral 25.0MG UNKNOWN UNKNOWN 0 25 MG
127062801 12706280 4 C XARELTO RIVAROXABAN 1 Oral 15.0MG UNKNOWN UNKNOWN 0 15 MG
127062801 12706280 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 137.0UG UNKNOWN UNKNOWN 0 137 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127062801 12706280 2 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127062801 12706280 Atrial fibrillation

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
127062801 12706280 2 201605 20160601 0