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
4429287 4196656 I 4429287-6 20040223 20040818 DIR 47 YR M N 358 LBS 20040817 PH Y N

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
4429287 1005126058 PS AUGMENTIN '125' 1 ORAL 400MG TID ORAL Y
4429287 1005145433 C MERTFORMIN 2
4429287 1005145434 C GLUCOTROL 1
4429287 1005145435 C HYDROCHLOROTHIAZIDE 1
4429287 1005145436 C LIPITOR 1
4429287 1005145437 C CHILDREN'S ASPIRIN 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4429287 1005126058 PNEUMONIA

Outcome of event

Event ID OUTC COD
4429287 HO

Reactions reported

Event ID PT
4429287 EXERCISE TOLERANCE DECREASED
4429287 FATIGUE
4429287 NEPHRITIS INTERSTITIAL
4429287 URINE FLOW DECREASED
4429287 URINE OUTPUT DECREASED

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
4429287 1005126058 20040207 20040223