The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6693104 7369914 I 6693104-4 20090201 20100413 20100420 EXP TPA2010A02042 TAKEDA PHARMACEUTICALS NORTH AMERICA. 62 YR F N 182 LBS 20100419 OT UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6693104 1013552571 PS ACTOS 1 ORAL 30 MG, 1 IN 1 D, PER ORAL; 15 MG, 1 IN 1 D, PER ORAL D D 21073
6693104 1013589578 C VERAPAMIL 1
6693104 1013589579 C SYMBICORT 1
6693104 1013589580 C ALBUTEROL 1
6693104 1013589582 C PRAVACHOL 1
6693104 1013589583 C METFORMIN HCL 1
6693104 1013589584 C NOVALOG (INSULIN ASPART) 2
6693104 1013589586 C LANTUS 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6693104 1013552571 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6693104 HO
6693104 OT
6693104 RI

Reactions reported

Event ID PT
6693104 ARRHYTHMIA
6693104 CEREBROVASCULAR ACCIDENT
6693104 DEHYDRATION
6693104 DIABETIC KETOACIDOSIS
6693104 FALL
6693104 LETHARGY
6693104 PANCREATITIS

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

Event ID RPSR COD
6693104 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6693104 1013552571 20060101 20090101
6693104 1013552571 20090101