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
127708491 12770849 1 I 20160902 0 20160922 20160922 DIR FDA-CTU 0.00 N 0.00000 0 N 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
127708491 12770849 1 PS DILANTIN PHENYTOIN 1 Oral 100MG X 3 MOUTH N Y 20170904 0 100 MG TID
127708491 12770849 3 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 0
127708491 12770849 5 C PROMETHAZINE PROMETHAZINEPROMETHAZINE HYDROCHLORIDE 1 0
127708491 12770849 7 C QUETIAPINE. QUETIAPINE 1 0
127708491 12770849 9 C PHENOBARBITAL. PHENOBARBITAL 1 0
127708491 12770849 11 C DULOXETINE DR DULOXETINE 1 0
127708491 12770849 13 C MECLIZINE MECLIZINE HYDROCHLORIDE 1 0
127708491 12770849 15 C DILANTIN PHENYTOIN 1 0
127708491 12770849 17 C CLONAZEPAM. CLONAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127708491 12770849 1 Seizure

Outcome of event

Event ID CASEID OUTC COD
127708491 12770849 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127708491 12770849 Dizziness
127708491 12770849 Erectile dysfunction
127708491 12770849 Gait disturbance
127708491 12770849 Muscular weakness

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

no results found

Therapies reported

no results found