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
7582992 7801949 F 7582992-5 20110122 20110616 20110630 EXP BR-GENENTECH-313394 GNEFDAAERSPRD 44 YR F Y 77 KG 20110630 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
7582992 1016902956 PS RITUXAN 1 UNKNOWN UNK NOTREPORTED
7582992 1016902958 SS ACTEMRA 1 UNKNOWN UNK
7582992 1016902959 SS ADALIMUMAB 2 UNKNOWN UNK
7582992 1016902960 SS INFLIXIMAB 2 UNKNOWN UNK
7582992 1016902963 C PANTOPRAZOLE 1
7582992 1016902957 SS ACTEMRA 1 UNKNOWN UNK
7582992 1016902962 C METHOTREXATE 1
7582992 1016902961 C METICORTEN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7582992 1016902956 RHEUMATOID ARTHRITIS
7582992 1016902959 RHEUMATOID ARTHRITIS
7582992 1016902960 RHEUMATOID ARTHRITIS
7582992 1016902963 PRODUCT USED FOR UNKNOWN INDICATION
7582992 1016902957 RHEUMATOID ARTHRITIS
7582992 1016902962 PRODUCT USED FOR UNKNOWN INDICATION
7582992 1016902961 PRODUCT USED FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
7582992 OT
7582992 HO

Reactions reported

Event ID PT
7582992 ONYCHOMADESIS
7582992 HYPERSENSITIVITY
7582992 DRUG INEFFECTIVE
7582992 RHEUMATOID ARTHRITIS
7582992 DEPRESSION
7582992 DYSPNOEA
7582992 FEELING OF DESPAIR
7582992 NAIL INFECTION

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
7582992 1016902958 20110101
7582992 1016902957 20100917 20101220 95 DAY