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
126034611 12603461 1 I 20140801 20151015 20160728 20160728 EXP US-PFIZER INC-3055612 PFIZER 77.00 YR F Y 0.00000 20160728 OT CN US

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
126034611 12603461 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U UNK 11719
126034611 12603461 2 SS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, FREQ:1 WEEK; INTERVAL: 1 U 1023260 0 50 MG
126034611 12603461 3 SS ENBREL ETANERCEPT 1 50 MG, FREQ:1 WEEK; INTERVAL: 1 U 1023260 0 50 MG
126034611 12603461 4 SS FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK U UNK 0
126034611 12603461 5 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK U UNK 0
126034611 12603461 6 SS PROLIA DENOSUMAB 1 Unknown UNK U UNK 0
126034611 12603461 7 C CORTISONE CORTISONEHYDROCORTISONE 1 UNK 0 TABLET
126034611 12603461 8 C MEDROL METHYLPREDNISOLONE 1 UNK UNK 0
126034611 12603461 9 C CALCIUM CALCIUM 1 UNK 0
126034611 12603461 10 C MAGNESIUM MAGNESIUM 1 UNK 0
126034611 12603461 11 C PREDNISONE. PREDNISONE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126034611 12603461 1 Ankylosing spondylitis
126034611 12603461 2 Ankylosing spondylitis
126034611 12603461 3 Rheumatoid arthritis
126034611 12603461 4 Product used for unknown indication
126034611 12603461 5 Ankylosing spondylitis
126034611 12603461 6 Product used for unknown indication
126034611 12603461 7 Product used for unknown indication
126034611 12603461 8 Product used for unknown indication
126034611 12603461 9 Product used for unknown indication
126034611 12603461 10 Product used for unknown indication
126034611 12603461 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126034611 12603461 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126034611 12603461 Arthralgia
126034611 12603461 Arthropathy
126034611 12603461 Back pain
126034611 12603461 Bladder disorder
126034611 12603461 Blood urine present
126034611 12603461 Bone density abnormal
126034611 12603461 Cough
126034611 12603461 Drug ineffective
126034611 12603461 Fall
126034611 12603461 Gait disturbance
126034611 12603461 Injection site erythema
126034611 12603461 Injection site mass
126034611 12603461 Injection site pain
126034611 12603461 Injection site pruritus
126034611 12603461 Injection site reaction
126034611 12603461 Injection site warmth
126034611 12603461 Joint fluid drainage
126034611 12603461 Joint range of motion decreased
126034611 12603461 Joint swelling
126034611 12603461 Joint warmth
126034611 12603461 Knee deformity
126034611 12603461 Micturition urgency
126034611 12603461 Musculoskeletal discomfort
126034611 12603461 Oesophageal disorder
126034611 12603461 Pain
126034611 12603461 Sinus disorder
126034611 12603461 Sinusitis
126034611 12603461 Sleep apnoea syndrome
126034611 12603461 Spider vein
126034611 12603461 Tooth repair
126034611 12603461 Vascular rupture

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
126034611 12603461 2 20020101 0
126034611 12603461 3 20140712 0