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
126148362 12614836 2 F 201607 20160727 20160802 20160804 EXP US-LUNDBECK-DKLU2017012 LUNDBECK 86.95 YR M Y 73.00000 KG 20160805 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
126148362 12614836 1 PS NORTHERA DROXIDOPA 1 Oral U 203202 300 MG CAPSULE TID
126148362 12614836 2 SS NORTHERA DROXIDOPA 1 U 203202
126148362 12614836 3 SS NORTHERA DROXIDOPA 1 U 203202
126148362 12614836 4 SS GABAPENTIN. GABAPENTIN 1 Unknown 0
126148362 12614836 5 SS HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126148362 12614836 1 Orthostatic hypotension
126148362 12614836 2 Autonomic neuropathy
126148362 12614836 3 Postural orthostatic tachycardia syndrome
126148362 12614836 4 Product used for unknown indication
126148362 12614836 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126148362 12614836 OT
126148362 12614836 LT
126148362 12614836 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126148362 12614836 Asthenia
126148362 12614836 Blood pressure increased
126148362 12614836 Confusional state
126148362 12614836 Dehydration
126148362 12614836 Diarrhoea
126148362 12614836 Dizziness
126148362 12614836 Hypotension
126148362 12614836 Loss of consciousness
126148362 12614836 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
126148362 12614836 1 201604 0