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
6699476 7368227 F 6699476-9 20080403 20100427 20100427 EXP CA-GENENTECH-259806 GNEFDAAERSPRD 37 YR F Y 95.2 KG 20100427 CN SWITZERLAND

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
6699476 1013580979 PS XOLAIR 1 SUBCUTANEOUS 450 MG, Q2W UNKNOWN
6699476 1013580980 SS XOLAIR 1 SUBCUTANEOUS 450 MG, Q2W S0079
6699476 1013580981 SS XOLAIR 1 SUBCUTANEOUS 450 MG, Q2W S0079A
6699476 1013580982 C BENADRYL 1
6699476 1013580983 C CORTISONE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6699476 1013580979 ASTHMA
6699476 1013580982 IODINE ALLERGY
6699476 1013580983 IODINE ALLERGY

Outcome of event

Event ID OUTC COD
6699476 OT

Reactions reported

Event ID PT
6699476 ANXIETY
6699476 CYANOSIS
6699476 HEADACHE
6699476 HYPERSENSITIVITY
6699476 HYPERTENSION
6699476 SWELLING FACE
6699476 WEIGHT INCREASED

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6699476 1013580979 20051111
6699476 1013580980 20100330
6699476 1013580981 20100413