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
125402892 12540289 2 F 20160624 20160708 20160708 EXP US-CIPLA-2014US00321 CIPLA 0.00 Y 0.00000 20160708 OT COUNTRY NOT SPECIFIED 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
125402892 12540289 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U U 77955
125402892 12540289 2 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 5 MG, QD U U 77955 5 MG
125402892 12540289 3 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 10 MG, QD U U 77955 10 MG
125402892 12540289 4 SS FUROSEMIDE. FUROSEMIDE 1 Unknown UNK U U 0
125402892 12540289 5 SS FUROSEMIDE. FUROSEMIDE 1 Intravenous (not otherwise specified) 30 MG, BID U U 0 30 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125402892 12540289 1 Hypertension
125402892 12540289 4 Blood pressure increased
125402892 12540289 5 Swelling face

Outcome of event

Event ID CASEID OUTC COD
125402892 12540289 OT
125402892 12540289 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125402892 12540289 Drug ineffective
125402892 12540289 Malaise
125402892 12540289 Nephrotic syndrome
125402892 12540289 Pharyngeal erythema
125402892 12540289 White blood cell count increased

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

no results found

Therapies reported

no results found