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
125966802 12596680 2 F 2016 20160721 20160727 20160728 EXP US-UCBSA-2016027337 UCB 53.02 YR F Y 0.00000 20160728 PH 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
125966802 12596680 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 400 MG, EV 2 WEEKS(QOW) Y U 901158, NDC # 20474071081 125160 400 MG QOW
125966802 12596680 2 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) Y U 125160 200 MG QOW
125966802 12596680 3 C ACYCLOVIR. ACYCLOVIR 1 UNK U U 0
125966802 12596680 4 C CELECOXIB. CELECOXIB 1 UNK U U 0
125966802 12596680 5 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK U U 0
125966802 12596680 6 C ESTRADIOL. ESTRADIOL 1 UNK U U 0
125966802 12596680 7 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 UNK U U 0
125966802 12596680 8 C FOLIC ACID. FOLIC ACID 1 UNK U U 0
125966802 12596680 9 C GABAPENTIN. GABAPENTIN 1 UNK U U 0
125966802 12596680 10 C KETOROLAC KETOROLACKETOROLAC TROMETHAMINE 1 UNK U U 0
125966802 12596680 11 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK U U 0
125966802 12596680 12 C MELOXICAM. MELOXICAM 1 UNK U U 0
125966802 12596680 13 C METHOTREXATE. METHOTREXATE 1 UNK U U 0
125966802 12596680 14 C NAPROXEN. NAPROXEN 1 UNK U U 0
125966802 12596680 15 C PHENTERMINE. PHENTERMINE 1 UNK U U 0
125966802 12596680 16 C PREDNISONE. PREDNISONE 1 UNK U U 0
125966802 12596680 17 C RANITIDINE. RANITIDINE 1 UNK U U 0
125966802 12596680 18 C TRAMADOL. TRAMADOL 1 UNK U U 0
125966802 12596680 19 C VITAMIN D CHOLECALCIFEROL 1 UNK U U 0
125966802 12596680 20 C VITAMIN D3 CHOLECALCIFEROL 1 UNK U U 0
125966802 12596680 21 C Apremilast APREMILAST 1 UNK U 0
125966802 12596680 22 C ZOSTAVAX VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125966802 12596680 1 Psoriatic arthropathy
125966802 12596680 3 Product used for unknown indication
125966802 12596680 4 Product used for unknown indication
125966802 12596680 5 Product used for unknown indication
125966802 12596680 6 Product used for unknown indication
125966802 12596680 7 Product used for unknown indication
125966802 12596680 8 Product used for unknown indication
125966802 12596680 9 Product used for unknown indication
125966802 12596680 10 Product used for unknown indication
125966802 12596680 11 Product used for unknown indication
125966802 12596680 12 Product used for unknown indication
125966802 12596680 13 Product used for unknown indication
125966802 12596680 14 Product used for unknown indication
125966802 12596680 15 Product used for unknown indication
125966802 12596680 16 Product used for unknown indication
125966802 12596680 17 Product used for unknown indication
125966802 12596680 18 Product used for unknown indication
125966802 12596680 19 Product used for unknown indication
125966802 12596680 20 Product used for unknown indication
125966802 12596680 21 Product used for unknown indication
125966802 12596680 22 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125966802 12596680 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125966802 12596680 Drug ineffective
125966802 12596680 Headache
125966802 12596680 Herpes zoster

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
125966802 12596680 1 20160209 201603 0
125966802 12596680 2 201603 201606 0
125966802 12596680 21 20160628 0