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
6718161 7382593 I 6718161-8 20100430 20100510 EXP US-PFIZER INC-2010054851 PFIZERINC YR F Y 77 KG 20100507 UNITED STATES

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
6718161 1013658003 PS LIPITOR 1 ORAL 10 MG, 1X/DAY 020702
6718161 1013658004 SS LIPITOR 1 020702
6718161 1013658005 SS ACTOS 1 ORAL 15 MG, 1X/DAY
6718161 1013658006 C GLYBURIDE 1 ORAL 5 MG, 2X/DAY, WITH MEAL
6718161 1013658007 C LOTENSIN 1 ORAL 10 MG, 1X/DAY
6718161 1013658008 C LOTENSIN 1
6718161 1013658009 C METHOTREXATE 2 UNKNOWN UNK
6718161 1013658010 C ACETYLSALICYLIC ACID 2 UNKNOWN 81 MG, 1X/DAY
6718161 1013658011 C FOLIC ACID 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6718161 1013658003 HYPERLIPIDAEMIA
6718161 1013658004 METABOLIC SYNDROME
6718161 1013658005 TYPE 2 DIABETES MELLITUS
6718161 1013658006 TYPE 2 DIABETES MELLITUS
6718161 1013658007 TYPE 2 DIABETES MELLITUS
6718161 1013658008 METABOLIC SYNDROME
6718161 1013658010 CARDIOVASCULAR EVENT PROPHYLAXIS

Outcome of event

Event ID OUTC COD
6718161 OT

Reactions reported

Event ID PT
6718161 ABDOMINAL DISTENSION
6718161 CHROMATURIA
6718161 FLUID RETENTION
6718161 OEDEMA PERIPHERAL
6718161 PALPITATIONS
6718161 WEIGHT INCREASED

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
6718161 1013658003 20100204 20100331 56 DAY
6718161 1013658005 20100204 20100331 56 DAY
6718161 1013658006 20081212
6718161 1013658007 20080408