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
6744119 7361701 F 6744119-9 20100524 20100527 EXP B0646787A GLAXOSMITHKLINE 72 YR F Y 96.4 KG 20100527 CN UNITED KINGDOM

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
6744119 1013762623 PS ROSIGLITAZONE 1 UNKNOWN 4MG PER DAY 21071
6744119 1013762624 SS ROSIGLITAZONE 1 UNKNOWN 8MG PER DAY 021071
6744119 1013762625 SS SIMVASTATIN 1 ORAL
6744119 1013762626 SS PIOGLITAZONE 1 UNKNOWN 30MG PER DAY
6744119 1013762627 SS ATORVASTATIN 2 UNKNOWN
6744119 1013762628 SS FENOFIBRATE 2 UNKNOWN 160MG PER DAY
6744119 1013762629 SS ACTOS 1 30MG PER DAY
6744119 1013762630 SS UNKNOWN DRUG 2
6744119 1013762631 C ROSUVASTATIN 1
6744119 1013762632 C METFORMIN HYDROCHLORIDE 1 1.5G PER DAY

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
6744119 OT

Reactions reported

Event ID PT
6744119 HIGH DENSITY LIPOPROTEIN DECREASED
6744119 MYALGIA

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
6744119 1013762623 20050301
6744119 1013762624 20050601
6744119 1013762626 20070201 20070501 13 WK
6744119 1013762627 20040201
6744119 1013762628 20030501
6744119 1013762629 20070201 20070501 13 WK