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
6696449 7371455 I 6696449-7 20100317 20100406 20100421 EXP TUK2010A00051 TAKEDA PHARMACEUTICALS NORTH AMERICA. 54 YR M N 20100420 UNITED KINGDOM

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
6696449 1013567108 PS ACTOS 1 ORAL 15 MG (15 MG), ORAL N 21073
6696449 1013598212 C ASPIRIN 1
6696449 1013598213 C ATORVASTATIN CALCIUM 1
6696449 1013598214 C GLUCOPHAGE SR (METFORMIN HYDROCHLORIDE) 2
6696449 1013598215 C TRBESARTAN (IRBESARTAN) 2
6696449 1013598216 C ACETAMINOPHEN 1
6696449 1013598218 C SITAGLIPTIN 2
6696449 1013598219 C TADALAFIL (TADALAFIL) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6696449 1013567108 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6696449 DS

Reactions reported

Event ID PT
6696449 ARTHRALGIA
6696449 DEAFNESS UNILATERAL
6696449 EYELID OEDEMA
6696449 FATIGUE
6696449 HEADACHE
6696449 TINNITUS
6696449 VERTIGO

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

Event ID RPSR COD
6696449 FGN
6696449 HP
6696449 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6696449 1013567108 20100317 20100319 2 DAY