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
126197132 12619713 2 F 20160817 20160803 20160831 EXP JP-VALIDUS PHARMACEUTICALS LLC-JP-2016VAL002389 VALIDUS 82.00 YR F Y 0.00000 20160831 OT JP JP

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
126197132 12619713 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral UNK U UNKNOWN 16273
126197132 12619713 2 C NIFEDIPINE. NIFEDIPINE 1 UNK U 0
126197132 12619713 3 C UBIDECARENONE UBIDECARENONE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126197132 12619713 1 Cardiac failure chronic
126197132 12619713 2 Product used for unknown indication
126197132 12619713 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126197132 12619713 LT
126197132 12619713 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126197132 12619713 Abdominal pain
126197132 12619713 Blood pressure decreased
126197132 12619713 Dehydration
126197132 12619713 Gait disturbance
126197132 12619713 Intestinal ischaemia
126197132 12619713 Metabolic acidosis
126197132 12619713 Pain
126197132 12619713 Pallor
126197132 12619713 Vomiting

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

no results found

Therapies reported

no results found