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
5797496 6213779 F 6 5797496-X 20050803 20080616 20080630 EXP 8020817 UCB, INC. M N 18.5 KG 20080624 MD 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
5797496 1010120675 PS KEPPRA 1 TRANSPLACENTAL 3000 MG /D TRP D D 21035
5797496 1010152362 C PLAQUENIL 1
5797496 1010152363 C VITAMIN TAB 1
5797496 1010152364 C FOLIC ACID 1
5797496 1010152365 C LEXAPRO 1
5797496 1010152366 C CLONAZEPAM 2
5797496 1010152367 C TRILEPTAL 1
5797496 1010152368 C ZANTAC 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5797496 CA

Reactions reported

Event ID PT
5797496 CARDIAC MURMUR
5797496 DYSPHAGIA
5797496 FOOD INTOLERANCE
5797496 GASTRITIS
5797496 GASTROOESOPHAGEAL REFLUX DISEASE
5797496 KNEE DEFORMITY
5797496 MATERNAL DRUGS AFFECTING FOETUS
5797496 PHARYNGITIS STREPTOCOCCAL
5797496 SEBORRHOEIC DERMATITIS
5797496 UPPER RESPIRATORY TRACT INFECTION
5797496 VENTRICULAR SEPTAL DEFECT

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

Event ID RPSR COD
5797496 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5797496 1010120675 20050803 20060426