The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125663852 12566385 2 F 20160811 20160718 20160817 EXP PE-PFIZER INC-2016344217 PFIZER 61.00 YR F Y 0.00000 20160817 CN PE PE

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125663852 12566385 1 PS XANAX XR ALPRAZOLAM 1 2 TABLETS OF 1 MG PER DAY AND 3 OR 4 TABLETS DAILY OF 0.5 MG, AS NEEDED (DEPENDING ON MOOD AND ANXIE U 18276 1 MG QID
125663852 12566385 2 SS XANAX XR ALPRAZOLAM 1 U 18276
125663852 12566385 3 SS XANAX ALPRAZOLAM 1 0.5 MG, 3X/DAY U 18276 .5 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125663852 12566385 1 Fibromyalgia
125663852 12566385 2 Insomnia
125663852 12566385 3 Depression

Outcome of event

Event ID CASEID OUTC COD
125663852 12566385 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125663852 12566385 Anxiety
125663852 12566385 Disease recurrence
125663852 12566385 Drug ineffective
125663852 12566385 Gait disturbance
125663852 12566385 Movement disorder
125663852 12566385 Spinal pain

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125663852 12566385 3 2008 0