The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5797494 6690472 F 1 5797494-6 20080401 20080613 20080630 EXP 8033359 UCB, INC 43 YR F N 52.3 KG 20080620 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5797494 1010120670 PS KEPPRA 1 ORAL 3/D PO D D 21035
5797494 1010152157 SS KEPPRA 1 ORAL 1000 MG PO D D
5797494 1010152158 SS KEPPRA 1 ORAL 500 MG 3/D PO D D
5797494 1010152160 SS KEFLEX 1 500 MG 4/D N D
5797494 1010152230 C ZONEGRAN 1
5797494 1010152231 C LAMICTAL 1
5797494 1010152232 C PENICILLIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5797494 1010120670 CONVULSION
5797494 1010152157 CONVULSION
5797494 1010152158 CONVULSION
5797494 1010152160 INFECTION

Outcome of event

Event ID OUTC COD
5797494 OT

Reactions reported

Event ID PT
5797494 BACTERIAL RHINITIS
5797494 BLOODY DISCHARGE
5797494 CONVULSION
5797494 EPISTAXIS
5797494 NASAL CONGESTION
5797494 NASOPHARYNGITIS
5797494 STAPHYLOCOCCAL INFECTION
5797494 UPPER RESPIRATORY TRACT INFECTION
5797494 URINARY TRACT INFECTION

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

Event ID RPSR COD
5797494 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5797494 1010120670 20070601 20080101
5797494 1010152157 20080101 20080515
5797494 1010152158 20080515
5797494 1010152160 20080401 20080428