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
7205780 7387205 F 7205780-8 20100419 20101223 20101231 EXP CH-PFIZER INC-CH-WYE-H15077910 PFIZERINC 79 YR F Y 20101231 MD SWITZERLAND

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
7205780 1015450464 PS AMIODARONE HCL 1 ORAL 200 MG, 1X/DAY 018972
7205780 1015450465 SS TENORETIC 100 1 ORAL 50 MG, 1X/DAY
7205780 1015450466 SS LUDIOMIL 1 ORAL 75 MG, 1X/DAY
7205780 1015450467 SS TRAMAL 2 UNKNOWN UNK
7205780 1015450468 C XANAX 1
7205780 1015450469 C NEXIUM 1
7205780 1015450470 C FOLIC ACID 2
7205780 1015450471 C EUTHYROX 2
7205780 1015450472 C COZAAR 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
7205780 DE
7205780 OT

Reactions reported

Event ID PT
7205780 BRADYCARDIA
7205780 CARDIO-RESPIRATORY ARREST
7205780 DRUG INTERACTION
7205780 ELECTROCARDIOGRAM QT PROLONGED
7205780 HYPOXIC-ISCHAEMIC ENCEPHALOPATHY

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7205780 1015450464 20100419
7205780 1015450465 20100419
7205780 1015450466 20100419
7205780 1015450467 20100419