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
126220351 12622035 1 I 2015 20160729 20160804 20160804 EXP US-PFIZER INC-2016369340 PFIZER 0.00 F Y 0.00000 20160804 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
126220351 12622035 1 PS DILANTIN PHENYTOIN 1 UNK U 10151
126220351 12622035 2 SS KEPPRA LEVETIRACETAM 1 1000 MG, DAILY U 0 1000 MG
126220351 12622035 3 SS LAMICTAL LAMOTRIGINE 1 UNK, DAILY U 0
126220351 12622035 4 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK U 0
126220351 12622035 5 SS KLONOPIN CLONAZEPAM 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126220351 12622035 1 Generalised tonic-clonic seizure

Outcome of event

Event ID CASEID OUTC COD
126220351 12622035 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126220351 12622035 Coma
126220351 12622035 Drug ineffective
126220351 12622035 Head injury
126220351 12622035 Pain
126220351 12622035 Road traffic accident
126220351 12622035 Seizure

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

no results found

Therapies reported

no results found