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
6730241 7382593 F 6730241-X 20100301 20100510 20100518 EXP US-PFIZER INC-2010054851 PFIZERINC 61 YR F Y 76.644 KG 20100518 OT 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
6730241 1013707013 PS LIPITOR 1 ORAL 10 MG, 1X/DAY 020702
6730241 1013707014 SS LIPITOR 1 020702
6730241 1013707015 SS ACTOS 1 ORAL 15 MG, 1X/DAY
6730241 1013707016 C GLYBURIDE 1 ORAL 5 MG, 2X/DAY, WITH MEAL
6730241 1013707017 C LOTENSIN 1 ORAL 10 MG, 1X/DAY
6730241 1013707018 C LOTENSIN 1
6730241 1013707019 C METHOTREXATE 2 UNKNOWN UNK
6730241 1013707020 C ACETYLSALICYLIC ACID 2 UNKNOWN 81 MG, 1X/DAY
6730241 1013707021 C FOLIC ACID 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6730241 1013707013 HYPERLIPIDAEMIA
6730241 1013707014 METABOLIC SYNDROME
6730241 1013707015 TYPE 2 DIABETES MELLITUS
6730241 1013707016 TYPE 2 DIABETES MELLITUS
6730241 1013707017 TYPE 2 DIABETES MELLITUS
6730241 1013707018 METABOLIC SYNDROME
6730241 1013707020 CARDIOVASCULAR EVENT PROPHYLAXIS

Outcome of event

Event ID OUTC COD
6730241 OT

Reactions reported

Event ID PT
6730241 ABDOMINAL DISTENSION
6730241 CHROMATURIA
6730241 FLUID RETENTION
6730241 OEDEMA PERIPHERAL
6730241 PALPITATIONS
6730241 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
6730241 1013707013 20100204 20100331 56 DAY
6730241 1013707015 20100204 20100331 56 DAY
6730241 1013707016 20081212
6730241 1013707017 20080408