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
124928362 12492836 2 F 20160620 20160623 20160713 PER US-PFIZER INC-2016196780 PFIZER 79.00 YR F Y 0.00000 20160713 CN 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
124928362 12492836 1 PS GABAPENTIN. GABAPENTIN 1 UNK 20235
124928362 12492836 2 SS NEURONTIN GABAPENTIN 1 UNK U 20235
124928362 12492836 3 C VFEND VORICONAZOLE 1 Oral 200MG, EVERY 12 HOURS 0 200 MG
124928362 12492836 4 C VITAMIN B6 PYRIDOXINE HYDROCHLORIDE 1 UNK 0
124928362 12492836 5 C VITAMIN D CHOLECALCIFEROL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124928362 12492836 1 Hypoaesthesia
124928362 12492836 2 Hypoaesthesia
124928362 12492836 3 Bronchopulmonary aspergillosis
124928362 12492836 4 Vitamin B6 deficiency
124928362 12492836 5 Vitamin D deficiency

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124928362 12492836 Product use issue
124928362 12492836 Visual impairment

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
124928362 12492836 3 2015 201603 0
124928362 12492836 4 2015 0
124928362 12492836 5 2015 0