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
126976211 12697621 1 I 20151106 20160830 20160830 EXP DK-MYLANLABS-2015M1039339 MYLAN 0.00 Y 0.00000 20160830 CN DK DK

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
126976211 12697621 1 PS LAMOTRIGINE. LAMOTRIGINE 1 UNK U U 76630
126976211 12697621 2 SS LEVETIRACETAM. LEVETIRACETAM 1 2 MG, UNK U U 0 2 MG
126976211 12697621 3 SS LEVETIRACETAM ^STADA^ LEVETIRACETAM 1 UNK U U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126976211 12697621 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126976211 12697621 Amnesia
126976211 12697621 Balance disorder
126976211 12697621 Chest discomfort
126976211 12697621 Decreased appetite
126976211 12697621 Disturbance in attention
126976211 12697621 Dizziness
126976211 12697621 Dyspnoea
126976211 12697621 Eye pain
126976211 12697621 Fatigue
126976211 12697621 Hypersomnia
126976211 12697621 Hyperventilation
126976211 12697621 Impaired work ability
126976211 12697621 Lethargy
126976211 12697621 Malaise
126976211 12697621 Poisoning
126976211 12697621 Presyncope
126976211 12697621 Psychomotor skills impaired
126976211 12697621 Somnolence
126976211 12697621 Vision blurred
126976211 12697621 Visual impairment

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
126976211 12697621 2 20141230 0