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
6702898 7325680 F 6702898-0 20100201 20100420 20100429 EXP US-NOVOPROD-305375 NOVOPROD 69 YR M Y 69.841 KG 20100430 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
6702898 1013596471 PS LEVEMIR 1 SUBCUTANEOUS 10 U, QD 021536
6702898 1013596472 SS LEVEMIR 1 SUBCUTANEOUS 15 IU, QD UNKNOWN 021536
6702898 1013596473 SS LEVEMIR 1 SUBCUTANEOUS 13 IU, QD 021536
6702898 1013596474 SS ACTOS 1 ORAL 15 MG, QD
6702898 1013596475 SS ACTOS 1 ORAL 30 MG, QD
6702898 1013596476 C METFORMIN 2 ORAL UNK
6702898 1013596477 C METFORMIN 2 ORAL 2000 MG, QD
6702898 1013596478 C LEVOTHYROXINE 2 UNK
6702898 1013596479 C ASPIRIN 1 ORAL UNK
6702898 1013596480 C SIMVASTATIN 1 ORAL UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6702898 1013596471 TYPE 2 DIABETES MELLITUS
6702898 1013596474 TYPE 2 DIABETES MELLITUS
6702898 1013596476 TYPE 2 DIABETES MELLITUS
6702898 1013596478 HYPOTHYROIDISM
6702898 1013596479 PROPHYLAXIS
6702898 1013596480 HYPERLIPIDAEMIA

Outcome of event

Event ID OUTC COD
6702898 HO

Reactions reported

Event ID PT
6702898 BLOOD GLUCOSE DECREASED
6702898 BLOOD GLUCOSE INCREASED
6702898 LOSS OF CONSCIOUSNESS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6702898 1013596471 20091221
6702898 1013596472 20100115 20100218 34 DAY
6702898 1013596473 20100222
6702898 1013596474 20091221 20100214 55 DAY
6702898 1013596475 20100215 20100220 5 DAY
6702898 1013596477 20100222
6702898 1013596478 20080101