The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
117134027 11713402 7 F 201510 20160727 20151109 20160808 EXP CA-JNJFOC-20151024045 JOHNSON AND JOHNSON 61.00 YR A F Y 0.00000 20160808 MD CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
117134027 11713402 1 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown 4 X N U UNKNOWN 0 500 MG UNSPECIFIED
117134027 11713402 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown X 8 N U UNKNOWN 0 500 MG UNSPECIFIED
117134027 11713402 3 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown N U UNKNOWN 0 UNSPECIFIED
117134027 11713402 4 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown 4 X N U UNKNOWN 0 500 MG UNSPECIFIED
117134027 11713402 5 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown X 8 N U UNKNOWN 19872 500 MG UNSPECIFIED
117134027 11713402 6 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown N U UNKNOWN 19872 UNSPECIFIED
117134027 11713402 7 SS XELJANZ TOFACITINIB CITRATE 1 Oral N 0 TABLET
117134027 11713402 8 SS XELJANZ TOFACITINIB CITRATE 1 Oral N 0 5 MG TABLET BID
117134027 11713402 9 SS XELJANZ TOFACITINIB CITRATE 1 Oral N 0 5 MG TABLET BID
117134027 11713402 10 SS XELJANZ TOFACITINIB CITRATE 1 Oral N 0 5 MG TABLET BID
117134027 11713402 11 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral N 0 TABLET
117134027 11713402 12 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral N 0 20 MG TABLET
117134027 11713402 13 SS CELEBREX CELECOXIB 1 Oral N 0 200 MG CAPSULE, HARD BID
117134027 11713402 14 SS CELEBREX CELECOXIB 1 Oral TO 200MG DIE (DAILY) FROM 200MG BID N 0 200 MG CAPSULE, HARD
117134027 11713402 15 SS LYRICA PREGABALIN 1 Oral 0 CAPSULE, HARD
117134027 11713402 16 SS CORTISONE CORTISONEHYDROCORTISONE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117134027 11713402 1 Pain
117134027 11713402 2 Pain
117134027 11713402 3 Pain
117134027 11713402 4 Rheumatoid arthritis
117134027 11713402 5 Rheumatoid arthritis
117134027 11713402 6 Rheumatoid arthritis
117134027 11713402 7 Rheumatoid arthritis
117134027 11713402 8 Rheumatoid arthritis
117134027 11713402 9 Rheumatoid arthritis
117134027 11713402 10 Rheumatoid arthritis
117134027 11713402 11 Rheumatoid arthritis
117134027 11713402 12 Rheumatoid arthritis
117134027 11713402 13 Rheumatoid arthritis
117134027 11713402 14 Rheumatoid arthritis
117134027 11713402 15 Product used for unknown indication
117134027 11713402 16 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
117134027 11713402 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117134027 11713402 Alopecia
117134027 11713402 Bladder cancer
117134027 11713402 Haemorrhage urinary tract
117134027 11713402 Hepatic enzyme increased
117134027 11713402 Middle insomnia
117134027 11713402 Pain
117134027 11713402 Poor quality sleep
117134027 11713402 Urinary incontinence
117134027 11713402 Urinary tract infection

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
117134027 11713402 8 20151019 20160104 0
117134027 11713402 9 20150825 20151004 0
117134027 11713402 10 20150806 20150811 0
117134027 11713402 12 201504 201508 0