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
127043012 12704301 2 F 20101208 20160825 20160831 20160902 EXP US-ASTRAZENECA-2010BM13281 ASTRAZENECA 21538.00 DY M Y 127.00000 KG 20160903 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
127043012 12704301 1 PS SYMLIN PRAMLINTIDE ACETATE 1 Subcutaneous 21332 15 UG INJECTION TID
127043012 12704301 2 SS BYDUREON EXENATIDE 1 Subcutaneous FN0141 0 2 MG /wk
127043012 12704301 3 C LISINOPRIL. LISINOPRIL 1 0 45 MG BID
127043012 12704301 4 C LASIX FUROSEMIDE 1 0 120 MG QD
127043012 12704301 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK 0 TABLET
127043012 12704301 6 C NOVOLOG INSULIN ASPART 1 Subcutaneous DOSE UNIT:45, THREE TIMES A DAY 0
127043012 12704301 7 C LANTUS INSULIN GLARGINE 1 Subcutaneous DOSE UNIT:80, EVERY DAY 0
127043012 12704301 8 C LANTUS INSULIN GLARGINE 1 Subcutaneous DOSE UNIT:90 0
127043012 12704301 9 C XARELTO RIVAROXABAN 1 Unknown UNK 0
127043012 12704301 10 C BLOOD PRESSURE MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127043012 12704301 1 Type 2 diabetes mellitus
127043012 12704301 2 Type 2 diabetes mellitus
127043012 12704301 4 Cardiac disorder
127043012 12704301 6 Diabetes mellitus
127043012 12704301 7 Diabetes mellitus
127043012 12704301 8 Diabetes mellitus
127043012 12704301 9 Anticoagulant therapy
127043012 12704301 10 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
127043012 12704301 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127043012 12704301 Atrial fibrillation
127043012 12704301 Blood pressure increased
127043012 12704301 Device malfunction
127043012 12704301 Dysgeusia

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
127043012 12704301 1 20101208 0
127043012 12704301 2 2015 0