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
124477192 12447719 2 F 201509 20160629 20160608 20160705 EXP US-UCBSA-2016020897 UCB 58.28 YR F Y 0.00000 20160705 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
124477192 12447719 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW), NDC NUMBER: 50474-0710-79 Y 901706 125160 200 MG SOLUTION FOR INJECTION QOW
124477192 12447719 2 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 3 WEEKS Y 125160 200 MG SOLUTION FOR INJECTION Q3W
124477192 12447719 3 C LATANOPROST. LATANOPROST 1 Ophthalmic 0.005 %, UNK U 0 .005 PCT EYE DROPS
124477192 12447719 4 C ALTACE RAMIPRIL 1 UNK, FREQUENCY : DAILY U 0
124477192 12447719 5 C Clobetasol CLOBETASOL 1 Topical UNK U 0
124477192 12447719 6 C CALCIPOTRIENE. CALCIPOTRIENE 1 Topical UNK U 0
124477192 12447719 7 C TOBRAMYCIN. TOBRAMYCIN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124477192 12447719 1 Rheumatoid arthritis
124477192 12447719 3 Glaucoma
124477192 12447719 4 Hypertension
124477192 12447719 5 Psoriasis
124477192 12447719 6 Psoriasis
124477192 12447719 7 Keratitis

Outcome of event

Event ID CASEID OUTC COD
124477192 12447719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124477192 12447719 Keratitis
124477192 12447719 Off label use
124477192 12447719 Oropharyngeal pain

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
124477192 12447719 1 201401 2016 0
124477192 12447719 2 201605 0