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
4871960 5959439 I 4871960-X 20051108 20051220 20051230 EXP T05-USA-05144-01 FOREST LABORATORIES INC. 87 YR F N 116 LBS 20051229 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
4871960 1006786238 PS MEMANTINE HCL 1 ORAL 4 TABLET QD PO Y D 21487
4871960 1006813166 SS MEMANTINE HCL 1 ORAL 4 TABLET QD PO D D
4871960 1006813167 C NORVASC 1
4871960 1006813168 C OSTEOBIFLEX 2
4871960 1006813169 C PRINIVIL 1
4871960 1006813170 C MULTI-VITAMIN 1
4871960 1006813171 C ASPIRIN 1
4871960 1006813173 C LIDODERM (LIDOCAINE) 2
4871960 1006813176 C ARICEPT 1
4871960 1006813177 C KADIAN 1
4871960 1006813178 C PLAVIX 1
4871960 1006813179 C DARVOCET 1
4871960 1006813182 C SYNTHROID 1
4871960 1006813184 C AMBIEN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4871960 1006786238 DEMENTIA ALZHEIMER'S TYPE
4871960 1006813166 DEMENTIA ALZHEIMER'S TYPE

Outcome of event

Event ID OUTC COD
4871960 HO

Reactions reported

Event ID PT
4871960 ANION GAP DECREASED
4871960 BACK PAIN
4871960 BLOOD ALBUMIN DECREASED
4871960 BLOOD CHLORIDE INCREASED
4871960 BLOOD GLUCOSE INCREASED
4871960 BLOOD POTASSIUM INCREASED
4871960 BLOOD PRESSURE DIASTOLIC INCREASED
4871960 COLD SWEAT
4871960 CONFUSIONAL STATE
4871960 DROOLING
4871960 HAEMOGLOBIN DECREASED
4871960 HYPOTENSION
4871960 LETHARGY
4871960 LOSS OF CONSCIOUSNESS
4871960 MALAISE
4871960 MENTAL STATUS CHANGES
4871960 PANCREATITIS
4871960 PCO2 DECREASED
4871960 PROTEIN TOTAL DECREASED
4871960 RENAL FAILURE ACUTE
4871960 UNRESPONSIVE TO VERBAL STIMULI
4871960 URINARY TRACT INFECTION

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

Event ID RPSR COD
4871960 HP
4871960 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4871960 1006786238 20050823 20051108
4871960 1006813166 20051122