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
124840283 12484028 3 F 20151102 20160627 20160621 20160708 EXP GB-SA-2016SA113504 AVENTIS 70.00 YR E F Y 0.00000 20160708 CN GB GB

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
124840283 12484028 1 PS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown FOUR TIMES A WEEK Y UNKNOWN 20905 /cycle
124840283 12484028 2 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown MONDAYS, WEDNESDAYS AND FRIDAYS Y UNKNOWN 20905 10 MG /cycle
124840283 12484028 3 SS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY?SOLUTION FOR INJECTION IN PRE-FILLED PEN 1071.72 MG Y L76737 0 50 MG SOLUTION FOR INJECTION /wk
124840283 12484028 4 SS ENBREL ETANERCEPT 1 Unknown UNK?SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 1071.72 MG Y M72573 0 50 MG SOLUTION FOR INJECTION /wk
124840283 12484028 5 C ADCAL CALCIUM CARBONATE 1 Unknown UNK 0
124840283 12484028 6 C CANDESARTAN CANDESARTAN 1 Unknown UNK 0
124840283 12484028 7 C CELEBREX CELECOXIB 1 Unknown 100 MG, TWICE DAILY 0 100 MG BID
124840283 12484028 8 C DOXAZOSIN DOXAZOSINDOXAZOSIN MESYLATE 1 Unknown UNK 0
124840283 12484028 9 C LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown UNK 0
124840283 12484028 10 C PREDNISOLONE. PREDNISOLONE 1 Unknown 4 MG, DAILY 0 4 MG QD
124840283 12484028 11 C TOLTERODINE TOLTERODINE 1 Unknown 4 MG, DAILY 0 4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124840283 12484028 1 Rheumatoid arthritis
124840283 12484028 2 Rheumatoid arthritis
124840283 12484028 3 Rheumatoid arthritis
124840283 12484028 4 Rheumatoid arthritis
124840283 12484028 5 Osteopenia
124840283 12484028 6 Hypertension
124840283 12484028 7 Rheumatoid arthritis
124840283 12484028 8 Hypertension
124840283 12484028 9 Prophylaxis against gastrointestinal ulcer
124840283 12484028 10 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124840283 12484028 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124840283 12484028 Atrial fibrillation
124840283 12484028 Blood pressure increased
124840283 12484028 Cardiac failure
124840283 12484028 Diarrhoea
124840283 12484028 Heart rate irregular
124840283 12484028 Injection site rash
124840283 12484028 Joint dislocation
124840283 12484028 Osteoarthritis
124840283 12484028 Palpitations
124840283 12484028 Rash
124840283 12484028 Sluggishness

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
124840283 12484028 2 20141210 0
124840283 12484028 3 20150602 0
124840283 12484028 4 20160204 0
124840283 12484028 5 2010 0
124840283 12484028 6 2010 0
124840283 12484028 7 1996 0
124840283 12484028 8 2011 0
124840283 12484028 9 2000 0
124840283 12484028 10 199609 0