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
4871962 5926281 F 2 4871962-3 20051221 20051230 EXP S05-USA-04746-01 FOREST LABORATORIES INC. 82 YR F N 50.5 KG 20051229 MD 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
4871962 1006786240 PS LEXAPRO 1 Y D 21323
4871962 1006814537 SS DEMADEX 1 Y D
4871962 1006814540 SS ZIAC 1 Y D
4871962 1006814542 C NORVASC 1
4871962 1006814544 C SEROQUEL 1
4871962 1006814547 C ASPIRIN 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4871962 1006786240 DEPRESSION

Outcome of event

Event ID OUTC COD
4871962 HO

Reactions reported

Event ID PT
4871962 ACUTE PRERENAL FAILURE
4871962 AGITATION
4871962 ANAEMIA
4871962 AZOTAEMIA
4871962 BLOOD BICARBONATE INCREASED
4871962 BLOOD CHLORIDE DECREASED
4871962 BLOOD GLUCOSE INCREASED
4871962 CONDITION AGGRAVATED
4871962 DEPRESSION
4871962 HYPOVOLAEMIA
4871962 INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION
4871962 MENTAL DISORDER
4871962 METABOLIC ALKALOSIS
4871962 NEPHROSCLEROSIS
4871962 ORAL INTAKE REDUCED
4871962 PARANOIA
4871962 RENAL FAILURE CHRONIC
4871962 SKIN TURGOR DECREASED
4871962 SPECIFIC GRAVITY URINE INCREASED
4871962 WEIGHT DECREASED

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4871962 CR
4871962 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4871962 1006786240 20050901 20051003
4871962 1006814537 20050901 20051003
4871962 1006814540 20040101 20051003