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
126438121 12643812 1 I 201607 20160809 20160811 20160811 EXP US-PFIZER INC-2016381490 PFIZER 87.00 YR M Y 0.00000 20160811 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
126438121 12643812 1 PS GABAPENTIN. GABAPENTIN 1 Unknown UNK U 20235
126438121 12643812 2 SS NORTHERA DROXIDOPA 1 Oral 900 MG, DAILY (300 MG,3 IN 1 D) 0 900 MG CAPSULE
126438121 12643812 3 SS NORTHERA DROXIDOPA 1 0 CAPSULE
126438121 12643812 4 SS NORTHERA DROXIDOPA 1 0 CAPSULE
126438121 12643812 5 SS HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126438121 12643812 2 Orthostatic hypotension
126438121 12643812 3 Autonomic neuropathy
126438121 12643812 4 Postural orthostatic tachycardia syndrome
126438121 12643812 5 Blood pressure increased

Outcome of event

Event ID CASEID OUTC COD
126438121 12643812 LT
126438121 12643812 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126438121 12643812 Asthenia
126438121 12643812 Blood pressure increased
126438121 12643812 Confusional state
126438121 12643812 Dehydration
126438121 12643812 Diarrhoea
126438121 12643812 Dizziness
126438121 12643812 Hypotension
126438121 12643812 Urinary incontinence

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
126438121 12643812 2 201604 0