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
6758786 7415155 I 6758786-7 20060523 20100524 20100603 EXP TCI2010A01861 TAKEDA PHARMACEUTICALS NORTH AMERICA. 51 YR F N 20100602 JAPAN

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
6758786 1013820026 PS ACTOS 1 ORAL 7.5 MG (7.5 MG, 1 IN 1 D) PER ORAL D
6758786 1013837969 SS PREDNISOLONE 1 ORAL 18 MG (9 MG, 2 IN 1 D) PER ORAL
6758786 1013837970 C LANSOPRAZOLE 1
6758786 1013837971 C NOVORAPID 30 MIX (INSULIN ASPART) 2
6758786 1013837974 C VERAPAMIL HYDROCHLORIDE 1
6758786 1013837975 C LASIX 1
6758786 1013837976 C CONIEL (BENIDIPINE HYDROCHLORIDE) 2
6758786 1013837978 C LOSARTAN POTASSIUM 1
6758786 1013837979 C COTRIM 1
6758786 1013837980 C IPD (SUPLATAST TOSILATE) 2
6758786 1013837981 C THEOLONG (THEOPHYLLINE) 2 21073

Indications of drugs used

Event ID DRUG SEQ INDI PT
6758786 1013820026 DIABETES MELLITUS
6758786 1013837969 ASTHMA
6758786 1013837969 EOSINOPHILIC PNEUMONIA CHRONIC

Outcome of event

Event ID OUTC COD
6758786 HO
6758786 OT

Reactions reported

Event ID PT
6758786 BLOOD PRESSURE INCREASED
6758786 CHEST X-RAY ABNORMAL
6758786 CONVULSION
6758786 FALL
6758786 FEMUR FRACTURE
6758786 GLYCOSYLATED HAEMOGLOBIN INCREASED
6758786 HYPOGLYCAEMIC COMA
6758786 NAUSEA
6758786 OSTEOPOROSIS
6758786 PALPITATIONS
6758786 PUTAMEN HAEMORRHAGE
6758786 VERTEBROBASILAR INSUFFICIENCY
6758786 VERTIGO
6758786 VOMITING

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

Event ID RPSR COD
6758786 FGN
6758786 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6758786 1013820026 20060502 20091201 3 YR
6758786 1013837969 19880101