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
118867074 11886707 4 F 20160620 20160104 20160711 PER US-PFIZER INC-2015478467 PFIZER 49.00 YR F Y 86.00000 KG 20160711 MD 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
118867074 11886707 1 PS LYRICA PREGABALIN 1 Oral 300 MG, 2X/DAY (IN THE AM AND AT NIGHT) Y 21446 300 MG BID
118867074 11886707 2 SS LYRICA PREGABALIN 1 400 MG, DAILY (250 MG IN THE MORNING AND 150 MG AT NIGHT) Y CU040201 21446 400 MG
118867074 11886707 3 C IBUPROFEN. IBUPROFEN 1 UNK 0
118867074 11886707 4 C TOPIRAMATE. TOPIRAMATE 1 UNK (AT ONE TIME) 0
118867074 11886707 5 C GABAPENTIN. GABAPENTIN 1 UNK (AT ONE TIME) 0
118867074 11886707 6 C INDOMETHACIN. INDOMETHACIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118867074 11886707 1 Trigeminal neuralgia
118867074 11886707 2 Neuralgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118867074 11886707 Anxiety
118867074 11886707 Cognitive disorder
118867074 11886707 Condition aggravated
118867074 11886707 Confusional state
118867074 11886707 Drug effect incomplete
118867074 11886707 Impaired work ability
118867074 11886707 Memory impairment
118867074 11886707 Stress
118867074 11886707 Vision blurred
118867074 11886707 Vomiting
118867074 11886707 Weight increased

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
118867074 11886707 1 2014 0
118867074 11886707 2 2015 0