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
81174983 8117498 3 F 20110808 20111212 20110901 20160910 EXP CA-UCBSA-039847 UCB 57.52 YR F Y 67.00000 KG 20160910 CN CA CA

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
81174983 8117498 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) 125160 200 MG QOW
81174983 8117498 2 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 400 MG ON WEEKS 0, 2 AND 4 58414 125160 400 MG QOW
81174983 8117498 3 SS GABAPENTIN. GABAPENTIN 1 300 MG, 3X/DAY (TID) Y 0 300 MG TID
81174983 8117498 4 SS SULFASALAZINE. SULFASALAZINE 1 Oral 1 G, 2X/DAY (BID) U 0 1 G BID
81174983 8117498 5 C ARAVA LEFLUNOMIDE 1 Oral 20 MG, ONCE DAILY (QD) 0 20 MG QD
81174983 8117498 6 C PREDNISONE. PREDNISONE 1 Oral 5 MG, ONCE DAILY (QD) 0 5 MG QD
81174983 8117498 7 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 200 MG, ONCE DAILY (QD) 0 200 MG QD
81174983 8117498 8 C FOLIC ACID. FOLIC ACID 1 Oral 5 MG, ONCE DAILY (QD) 0 5 MG QD
81174983 8117498 9 C MELOXICAM. MELOXICAM 1 Oral 7.5 MG, 2X/DAY (BID) 0 7.5 MG BID
81174983 8117498 10 C PARIET RABEPRAZOLE SODIUM 1 Oral 10 MG, 2X/DAY (BID) 0 10 MG BID
81174983 8117498 11 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 20 MG, ONCE DAILY (QD) 0 20 MG QD
81174983 8117498 12 C CALCIUM CALCIUM 1 Oral 1000 MG, ONCE DAILY (QD) 0 1000 MG QD
81174983 8117498 13 C RAMIPRIL. RAMIPRIL 1 Oral 10 MG, ONCE DAILY (QD) 0 10 MG QD
81174983 8117498 14 C ALDACTONE SPIRONOLACTONE 1 Oral 50 MG, ONCE DAILY (QD) 0 50 MG QD
81174983 8117498 15 C VITAMIN D CHOLECALCIFEROL 1 Oral 1000 IU, ONCE DAILY (QD) 0 1000 IU QD
81174983 8117498 16 C VITAMIN C ASCORBIC ACID 1 Oral 500 MG, ONCE DAILY (QD) 0 500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
81174983 8117498 1 Rheumatoid arthritis
81174983 8117498 3 Arthralgia
81174983 8117498 4 Rheumatoid arthritis
81174983 8117498 5 Rheumatoid arthritis
81174983 8117498 6 Rheumatoid arthritis
81174983 8117498 7 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
81174983 8117498 OT
81174983 8117498 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
81174983 8117498 Arthralgia
81174983 8117498 Dizziness
81174983 8117498 Herpes zoster
81174983 8117498 Nausea
81174983 8117498 Pancreatitis

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
81174983 8117498 1 20110714 0
81174983 8117498 2 20110602 20110630 0
81174983 8117498 3 20110816 0
81174983 8117498 4 2004 2011 0
81174983 8117498 5 2008 0
81174983 8117498 6 1978 0
81174983 8117498 7 1988 0