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
7387796 7480873 F 7387796-4 20080101 20110318 20110331 EXP BR-GENENTECH-303949 GNEFDAAERSPRD 53 YR F Y 76 KG 20110331 CN UNITED KINGDOM

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
7387796 1016144076 C METFORMIN HYDROCHLORIDE 1 500 MG, UNK
7387796 1016144074 C ARAVA 1 20 MG, UNK
7387796 1016144075 C HUMALOG 1 UNK
7387796 1016144072 PS RITUXIMAB 2 INTRAVENOUS 1000 MG, Q14D NOTREPORTED
7387796 1016144073 SS RITUXIMAB 2 INTRAVENOUS UNK NOTREPORTED
7387796 1016144077 C OMEPRAZOLE 1 20 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
7387796 1016144076 PRODUCT USED FOR UNKNOWN INDICATION
7387796 1016144074 PRODUCT USED FOR UNKNOWN INDICATION
7387796 1016144075 PRODUCT USED FOR UNKNOWN INDICATION
7387796 1016144072 RHEUMATOID ARTHRITIS
7387796 1016144077 PRODUCT USED FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
7387796 OT

Reactions reported

Event ID PT
7387796 DIABETES MELLITUS
7387796 ABASIA
7387796 ARTHRALGIA
7387796 DECUBITUS ULCER
7387796 SUFFOCATION FEELING
7387796 IMMUNODEFICIENCY
7387796 ARTHROPATHY

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
7387796 1016144072 20080901 20080915 15 DAY
7387796 1016144073 20100701