The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6387686 7139515 F 1 6387686-X 20090101 20090918 20090930 EXP 8051829 UCB, INC. 53 YR F N 90.7 KG 20090928 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6387686 1012374644 PS CIMZIA 1 SUBCUTANEOUS 400 MG SC D D
6387686 1012429624 C LIPITOR 1
6387686 1012429625 C ZYRTEC 1
6387686 1012429627 C LEXAPRO 1
6387686 1012429628 C TRAZODONE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6387686 1012374644 CROHN'S DISEASE

Outcome of event

Event ID OUTC COD
6387686 HO

Reactions reported

Event ID PT
6387686 AGEUSIA
6387686 ANOSMIA
6387686 ASTHENOPIA
6387686 DIARRHOEA
6387686 DRUG INEFFECTIVE
6387686 DRY EYE
6387686 DYSGEUSIA
6387686 HERNIA HIATUS REPAIR
6387686 WEIGHT DECREASED

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

Event ID RPSR COD
6387686 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6387686 1012374644 20090714