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
127770542 12777054 2 F 20160425 20160920 20160923 20160926 EXP FI-009507513-1609FIN010823 MERCK 81.11 YR F Y 0.00000 20160926 OT FI FI

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
127770542 12777054 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 2 DF, QD; TOTAL DAILY DOSE: 100/2000 MG D U 22044 2 DF FILM-COATED TABLET QD
127770542 12777054 2 C FURESIS FUROSEMIDE 1 FREQUENCY: 2 X 2 0 2 DF BID
127770542 12777054 3 C BISOPROLOL ACTAVIS BISOPROLOL 1 FREQUENCY: 1/2 X 1 0 TABLET QD
127770542 12777054 4 C MICARDIS TELMISARTAN 1 FREQUENCY: 1X1 0 1 DF TABLET QD
127770542 12777054 5 C BECLOMET EASYHALER 2 INHALATION; STRENGTH;: 400 UG/DOSE; FREQUENCY: 1 X 2-4; TOTAL DAILY DOSE: 800-1600 UG 0
127770542 12777054 6 C OMEPRAZOL ACTAVIS OMEPRAZOLE 1 FREQUENCY: 1 X 1 0 1 DF CAPSULE QD
127770542 12777054 7 C PRIMASPAN ASPIRIN 1 FREQUENCY: 1 X 1 0 1 DF TABLET QD
127770542 12777054 8 C ALLONOL ALLOPURINOL 1 FREQUENCY: 1 X 1 0 1 DF TABLET QD
127770542 12777054 9 C THYROXIN LEVOTHYROXINE 1 0
127770542 12777054 10 C PEGORION 2 FREQUENCY: 1 X 3 0 1 DF TID
127770542 12777054 11 C VISCOTEARS CARBOMER 1 STRENGTH: 2 MG/G; FREQUENCY: 1 X 3-4 0 EYE DROPS
127770542 12777054 12 C BUVENTOL EASYHALER ALBUTEROL SULFATE 1 INHALATION; STRENGTH: 200 UG/DOSE; FREQUENCY: 1-2 X 2-4 WHEN NEEDE; TOTAL DAILY DOSE: 400-1600 UG 0
127770542 12777054 13 C BEMETSON K 2 STRENGTH: 1/30 MG/G; FREQUENCY: 1 X 1-2 WHEN NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127770542 12777054 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127770542 12777054 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127770542 12777054 Anaemia
127770542 12777054 Cardiovascular insufficiency
127770542 12777054 Chest pain
127770542 12777054 Dizziness
127770542 12777054 Fall
127770542 12777054 Hypothermia
127770542 12777054 Lactic acidosis
127770542 12777054 Renal failure
127770542 12777054 Respiratory failure
127770542 12777054 Sepsis

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
127770542 12777054 1 201504 20160425 0