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
6474095 7236811 I 6474095-8 20090901 20090903 20091123 PER 8051524 UCB, INC. 56 YR F N 60.78 KG 20091030 OT 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
6474095 1012712873 PS CIMZIA 1 SUBCUTANEOUS 400 MG /M SC Y D 50611 20100101
6474095 1012785518 C PANTASA 2
6474095 1012785519 C EVISTA 1
6474095 1012785520 C B-12 LATINO 2
6474095 1012785521 C VITAMINS NOS 2
6474095 1012785522 C FISH OIL 2
6474095 1012785523 C CRANBERRY 2
6474095 1012785524 C IRON 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6474095 1012712873 CROHN'S DISEASE

Outcome of event

no results found

Reactions reported

Event ID PT
6474095 ABDOMINAL PAIN
6474095 CONSTIPATION
6474095 FLATULENCE
6474095 ILEUS
6474095 NAUSEA

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

Event ID RPSR COD
6474095 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6474095 1012712873 20090731