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
4833118 5931281 I 4833118-X 20050101 20051107 20051117 EXP 2005152021 PFIZER INC. 56 YR F N 174 LBS 20051116 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
4833118 1006645070 PS GABAPENTIN 1 ORAL 300 MG (100 MG, 3 IN 1 D), ORAL D D 20235
4833118 1006670712 SS LYRICA 1 ORAL 300 MG (150 MG,2 IN 1 D), ORAL D D
4833118 1006670714 C ANTIHYPERTENSIVES (ANTIHYPERTENSIVES) 2
4833118 1006670715 C ESTRADIOL 1
4833118 1006670717 C GLUCOSAMINE (GLUCOSAMINE) 2
4833118 1006670718 C ALL OTHER NON-THERAPEUTIC PRODUCTS (ALL OTHER NON-THERAPEUTIC PRODUCTS 2
4833118 1006670719 C NIACIN 1
4833118 1006670720 C TRICOR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4833118 1006645070 NEUROPATHY PERIPHERAL
4833118 1006670712 NEUROPATHY PERIPHERAL

Outcome of event

Event ID OUTC COD
4833118 OT

Reactions reported

Event ID PT
4833118 DRUG EFFECT DECREASED
4833118 FEELING ABNORMAL
4833118 KNEE OPERATION
4833118 MOBILITY DECREASED
4833118 NERVOUS SYSTEM DISORDER
4833118 PROCEDURAL PAIN
4833118 SOMNOLENCE
4833118 TREATMENT NONCOMPLIANCE

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

Event ID RPSR COD
4833118 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4833118 1006645070 20050901
4833118 1006670712 20051001 20051001