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
4833379 5787221 F 4833379-7 20050307 20051107 20051117 EXP GBWYE528623MAR05 WYETH PHARMACEUTICALS INC. 17 YR M N 20051116 OT UNITED KINGDOM

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
4833379 1006645554 PS EFFEXOR 1 ORAL SEE IMAGE, ORAL D D 20151
4833379 1006666155 SS CANNABIS (CANNABIS, , 0 2 D D
4833379 1006666166 SS EFFEXOR XR 1 ORAL SEE IMAGE, ORAL D D
4833379 1006666167 SS FLUOXETINE 1 ORAL 20MG 1 XPER 1 DAY D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
4833379 1006645554 DEPRESSION
4833379 1006666166 DEPRESSION
4833379 1006666167 DEPRESSION

Outcome of event

Event ID OUTC COD
4833379 HO
4833379 LT

Reactions reported

Event ID PT
4833379 AFFECT LABILITY
4833379 AGITATION
4833379 DEPRESSED MOOD
4833379 DRUG ABUSER
4833379 DRUG DOSE OMISSION
4833379 DRUG INTERACTION
4833379 DRUG WITHDRAWAL SYNDROME
4833379 ELEVATED MOOD
4833379 GRAND MAL CONVULSION
4833379 HYPOMANIA
4833379 LOGORRHOEA

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

Event ID RPSR COD
4833379 FGN
4833379 HP
4833379 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4833379 1006645554 20050301 20050306 6 DAY
4833379 1006645554 20050307 20050407 31 DAY
4833379 1006645554 20050407 20050620 75 DAY
4833379 1006645554 20050621
4833379 1006666166 20050101 20050101
4833379 1006666166 20050621
4833379 1006666167 20041110 20050301 112 DAY