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
125308611 12530861 1 I 20151028 20160706 20160706 EXP CA-PFIZER INC-2015369502 PFIZER 58.00 YR F Y 0.00000 20160706 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
125308611 12530861 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 20 MG, WEEKLY N 11719 20 MG /wk
125308611 12530861 2 SS LEFLUNOMIDE. LEFLUNOMIDE 1 20 MG, UNK N 0 20 MG
125308611 12530861 3 SS PREDNISONE. PREDNISONE 1 Oral UNK N 0
125308611 12530861 4 SS PREDNISONE. PREDNISONE 1 N 0
125308611 12530861 5 C PERINDOPRIL PERINDOPRIL 1 4 MG, DAILY 0 4 MG
125308611 12530861 6 C LIPITOR ATORVASTATIN CALCIUM 1 40 MG, 1X/DAY 0 40 MG TABLET QD
125308611 12530861 7 C METFORMIN METFORMIN HYDROCHLORIDE 1 500 MG, 2X/DAY 0 500 MG BID
125308611 12530861 8 C METOPROLOL. METOPROLOL 1 75 MG, 2X/DAY 0 75 MG BID
125308611 12530861 9 C PANTOLOC /01263204/ PANTOPRAZOLE SODIUM 1 40 MG, 1X/DAY 0 40 MG QD
125308611 12530861 10 C FOLIC ACID. FOLIC ACID 1 5 MG, WEEKLY 0 5 MG /wk
125308611 12530861 11 C FERROUS FUMARATE FERROUS FUMARATE 1 300 MG, DAILY 0 300 MG
125308611 12530861 12 C ASA ASPIRIN 1 81 MG, 1X/DAY 0 81 MG QD
125308611 12530861 13 C TRAVOPROST TRAVOPROST 1 UNK 0 EYE DROPS
125308611 12530861 14 C DEPO-MEDROL METHYLPREDNISOLONE ACETATE 1 UNK 0
125308611 12530861 15 C XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125308611 12530861 1 Rheumatoid arthritis
125308611 12530861 2 Rheumatoid arthritis
125308611 12530861 3 Rheumatoid arthritis
125308611 12530861 4 Pain
125308611 12530861 14 Rheumatoid arthritis
125308611 12530861 15 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125308611 12530861 OT
125308611 12530861 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125308611 12530861 Condition aggravated
125308611 12530861 Decreased appetite
125308611 12530861 Drug ineffective
125308611 12530861 Haemoglobin decreased
125308611 12530861 Hypoglycaemia
125308611 12530861 Nasal disorder
125308611 12530861 Oral disorder
125308611 12530861 Rheumatoid arthritis
125308611 12530861 Sweating fever
125308611 12530861 Synovitis
125308611 12530861 Ulcer
125308611 12530861 Weight fluctuation

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
125308611 12530861 1 201304 201601 0
125308611 12530861 2 201408 201410 0
125308611 12530861 3 201510 0
125308611 12530861 15 20141212 0