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
126095591 12609559 1 I 2014 20160316 20160801 20160801 PER US-TEVA-644751USA TEVA 0.00 F Y 59.02000 KG 20160801 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
126095591 12609559 1 PS BACLOFEN. BACLOFEN 1 Oral 10 MILLIGRAM DAILY; Y 72234 10 MG QD
126095591 12609559 2 SS AMPYRA DALFAMPRIDINE 1 Oral 20 MILLIGRAM DAILY; Y 0 10 MG TABLET BID
126095591 12609559 3 C NIFEDIPINE. NIFEDIPINE 1 60 MILLIGRAM DAILY; 0 30 MG BID
126095591 12609559 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 75 MICROGRAM DAILY; 0 75 UG QD
126095591 12609559 5 C GABAPENTIN. GABAPENTIN 1 400 MILLIGRAM DAILY; 0 100 MG QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126095591 12609559 1 Product used for unknown indication
126095591 12609559 2 Gait disturbance

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126095591 12609559 Dizziness
126095591 12609559 Drug intolerance
126095591 12609559 Gait disturbance

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
126095591 12609559 1 2014 0
126095591 12609559 2 201003 0
126095591 12609559 3 2006 0
126095591 12609559 4 1990 0
126095591 12609559 5 2011 0