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
100234881 10023488 1 I 20120416 20131217 20131231 20131231 EXP 2013SA091144 SANOFI 64.00 YR F N 69.50000 KG 20131230 N JP

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
100234881 10023488 1 PS MYSLEE 1 ORAL Y D 19908 5 MG TABLET PRN
100234881 10023488 2 SS PROGRAF (TACROLIMUS) 1 ORAL N D 0 1 MG QD
100234881 10023488 3 SS CERTOLIZUMAB PEGOL (CERTOLIZUMAB PEGOL) 1 SUBCUTANEOUS N D 0 200 MG
100234881 10023488 4 SS RHEUMATREX 1 ORAL N D 0 10 MG QD
100234881 10023488 5 SS PREDNISOLONE (PREDNISOLONE) 1 ORAL N D 0 2.5 MG QD
100234881 10023488 6 SS PREDNISOLONE (PREDNISOLONE) 1 ORAL N D 0 1 MG QD
100234881 10023488 7 SS CEFZON 1 ORAL D D 0 100 MG TID
100234881 10023488 8 SS EQUA 1 ORAL D D 0 50 MG QD
100234881 10023488 10 C LOXONIN 1 0
100234881 10023488 12 C FOLIAMIN 1 0
100234881 10023488 14 C MUCOSTA 1 0
100234881 10023488 16 C CALBLOCK 1 0
100234881 10023488 18 C VALSARTAN 1 0
100234881 10023488 20 C METHYYCOBAL 2 0
100234881 10023488 22 C ALINAMIN F 1 0
100234881 10023488 24 C CRESTOR 1 0
100234881 10023488 26 C VOLTAREN 1 0
100234881 10023488 28 C ROCEPHIN 1 0
100234881 10023488 30 C ACETAMINOPHEN 1 0
100234881 10023488 32 C ZITHROMAC 1 0
100234881 10023488 34 C PRIMPERAN 1 0
100234881 10023488 36 C MEROPENEM 1 0
100234881 10023488 38 C CALONAL 1 0
100234881 10023488 40 C NOVORAPID 1 0
100234881 10023488 42 C BIOFERMIN R 1 0
100234881 10023488 44 C PARIET 1 0
100234881 10023488 46 C CEFTRIAXONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100234881 10023488 1 Insomnia
100234881 10023488 2 Rheumatoid arthritis
100234881 10023488 3 Rheumatoid arthritis
100234881 10023488 4 Rheumatoid arthritis
100234881 10023488 5 Rheumatoid arthritis
100234881 10023488 6 Rheumatoid arthritis
100234881 10023488 7 Product used for unknown indication
100234881 10023488 8 Diabetes mellitus management

Outcome of event

Event ID CASEID OUTC COD
100234881 10023488 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100234881 10023488 Intentional drug misuse
100234881 10023488 Pyelonephritis acute

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

Event ID CASEID RPSR COD
100234881 10023488 FGN
100234881 10023488 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
100234881 10023488 1 20120416 498 DAY
100234881 10023488 2 20130704 20130828 0
100234881 10023488 3 20121025 0
100234881 10023488 4 20130315 20130828 0
100234881 10023488 5 20120621 20130828 0
100234881 10023488 6 20120621 20130828 0
100234881 10023488 7 20130907 20130909 0
100234881 10023488 8 20130906 20130909 0