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
127182231 12718223 1 I 201308 20160822 20160906 20160906 PER US-ASTRAZENECA-2016SE90690 ASTRAZENECA 409.00 MON F Y 83.90000 KG 20160906 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
127182231 12718223 1 PS BYDUREON EXENATIDE 1 Unknown ONCE A WEEK Y 22200
127182231 12718223 2 SS SYMLIN PRAMLINTIDE ACETATE 1 Subcutaneous 15 MCG, THREE TIMES A DAY WITH MEALS Y U 0 INJECTION
127182231 12718223 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 0 1000 MG Q12H
127182231 12718223 4 C VICTOZA LIRAGLUTIDE 1 0
127182231 12718223 5 C BUPROPION. BUPROPION 1 Oral 0 150 MG QD
127182231 12718223 6 C XYZAL LEVOCETIRIZINE DIHYDROCHLORIDE 1 Oral 0 5 MG QD
127182231 12718223 7 C HUMALOG INSULIN LISPRO 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127182231 12718223 2 Insulin resistance
127182231 12718223 6 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127182231 12718223 Decreased appetite
127182231 12718223 Diarrhoea
127182231 12718223 Nausea
127182231 12718223 Weight decreased
127182231 12718223 Weight increased

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
127182231 12718223 2 201308 201405 0