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
8248636 8485919 I 8248636-4 20120101 20120316 20120331 EXP BR-AMGEN-BRASP2012003994 AMGENSAFETY 57 YR F Y 70 KG 20120330 CN BRAZIL

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
8248636 1019282330 C PREDNISONE TAB 1 10 MG, 1X/DAY
8248636 1019282334 C DIAMICRON 2 THREE TABLETS DAILY
8248636 1019282332 C METFORMIN HCL 1 800 MG, 2X/DAY
8248636 1019282331 C SIMVASTATIN 1 20 MG, 2X/DAY
8248636 1019282328 PS ENBREL 1 SUBCUTANEOUS 50 MG, 1X/WEEK
8248636 1019282329 SS ENBREL 1 SUBCUTANEOUS 50 MG, 1X/WEEK
8248636 1019282335 C CORUS 2 ONE AT NIGHT
8248636 1019282333 C DIOSMIN 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248636 1019282330 PAIN
8248636 1019282334 DIABETES MELLITUS
8248636 1019282332 DIABETES MELLITUS
8248636 1019282328 RHEUMATOID ARTHRITIS
8248636 1019282335 HYPERTENSION

Outcome of event

Event ID OUTC COD
8248636 OT

Reactions reported

Event ID PT
8248636 PRURITUS GENERALISED
8248636 PRURITUS GENITAL
8248636 HYPERGLYCAEMIA
8248636 VARICOPHLEBITIS
8248636 ACNE
8248636 INFLUENZA

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
8248636 1019282330 20100101
8248636 1019282328 20120117
8248636 1019282329 20111201
8248636 1019282335 20100101