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
126487431 12648743 1 I 201606 20160801 20160812 20160812 PER US-PFIZER INC-2016370608 PFIZER 63.00 YR M Y 90.26000 KG 20160812 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
126487431 12648743 1 PS DILANTIN PHENYTOIN 1 100 MG, UNK 84349 100 MG CAPSULE, HARD
126487431 12648743 2 SS DILANTIN PHENYTOIN 1 300 MG, 2X/DAY(IN THE MORNING, AT NIGHT) 84349 300 MG CAPSULE, HARD BID
126487431 12648743 3 SS DILANTIN PHENYTOIN 1 200 MG, 1X/DAY(AT NIGHT) 84349 200 MG CAPSULE, HARD QD
126487431 12648743 4 C MYSOLINE PRIMIDONE 1 500 MG, 1X/DAY 0 500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126487431 12648743 1 Seizure
126487431 12648743 4 Seizure

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126487431 12648743 Aura
126487431 12648743 Condition aggravated
126487431 12648743 Constipation
126487431 12648743 Drug intolerance
126487431 12648743 Drug level decreased
126487431 12648743 Hypoaesthesia

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
126487431 12648743 4 1978 0