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
126616113 12661611 3 F 20160912 20160817 20160916 EXP US-PFIZER INC-2016387065 PFIZER 58.00 YR F Y 0.00000 20160916 CN US US

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
126616113 12661611 1 PS LYRICA PREGABALIN 1 100 MG, 3X/DAY Y N17614 21446 100 MG TID
126616113 12661611 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK U 0
126616113 12661611 3 C HORIZANT GABAPENTIN ENACARBIL 1 UNK 0
126616113 12661611 4 C COREG CARVEDILOL 1 UNK 0
126616113 12661611 5 C TRAMADOL. TRAMADOL 1 UNK 0
126616113 12661611 6 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 UNK 0
126616113 12661611 7 C MOBIC MELOXICAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126616113 12661611 1 Back pain
126616113 12661611 2 Pain

Outcome of event

Event ID CASEID OUTC COD
126616113 12661611 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126616113 12661611 Activities of daily living impaired
126616113 12661611 Condition aggravated
126616113 12661611 Dizziness
126616113 12661611 Fatigue
126616113 12661611 Oropharyngeal pain
126616113 12661611 Sinus congestion
126616113 12661611 Somnolence

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
126616113 12661611 1 201604 201608 0
126616113 12661611 3 201607 0