The Safety Rates Drug Report

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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
126044741 12604474 1 I 20160709 20160719 20160728 20160728 EXP GB-MHRA-TPP5362204C423755YC1468233368505 GB-MYLANLABS-2016M1030030 MYLAN 0.00 Y 0.00000 20160728 MD GB GB

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
126044741 12604474 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 UNK U U 76418
126044741 12604474 2 C ADALAT NIFEDIPINE 1 Oral 1 DF, QD 224.957993 DF U 0 1 DF QD
126044741 12604474 3 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 Oral 1 DF, QD (EACH MORNING) 2 DF U 0 1 DF QD
126044741 12604474 4 C LOSARTAN. LOSARTAN 1 Oral 1 DF, QD 256.958008 DF U 0 1 DF QD
126044741 12604474 5 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 DF, UNK (AS NECESSARY) U 0 2 DF

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126044741 12604474 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126044741 12604474 Eye pain
126044741 12604474 Headache
126044741 12604474 Photophobia

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
126044741 12604474 1 20160520 0
126044741 12604474 2 20151127 20160520 0
126044741 12604474 3 20160711 0
126044741 12604474 4 20151026 0
126044741 12604474 5 20151026 0