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
122042573 12204257 3 F 20160624 20160323 20160707 EXP GB-TEVA-645278ACC TEVA 0.00 F Y 0.00000 20160707 MD GB GB

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
122042573 12204257 1 PS LAMOTRIGINE. LAMOTRIGINE 1 Oral 200 MILLIGRAM DAILY; 200 MG, QD, 200 MILLIGRAM DAILY; Y U 76420 200 MG TABLET QD
122042573 12204257 2 SS LAMOTRIGINE. LAMOTRIGINE 1 Oral 150 MILLIGRAM DAILY; 100 MG, UNK, 150 MILLIGRAM DAILY; ONE 100MG TABLET AND HALF 100 MG TABLET Y U 76420 100 MG TABLET
122042573 12204257 3 SS LAMICTAL LAMOTRIGINE 1 Oral U 0 100 MG TABLET
122042573 12204257 4 SS LAMICTAL LAMOTRIGINE 1 Oral U 0 50 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122042573 12204257 1 Seizure
122042573 12204257 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122042573 12204257 OT
122042573 12204257 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122042573 12204257 Asthma
122042573 12204257 Dementia
122042573 12204257 Headache
122042573 12204257 Hypersensitivity
122042573 12204257 Infection
122042573 12204257 Nasal congestion
122042573 12204257 Seizure
122042573 12204257 Swelling face

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

no results found

Therapies reported

no results found