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
6698963 7328942 F 6698963-7 20100310 20100416 20100427 EXP B0641975A GLAXOSMITHKLINE 66 YR F Y 62 KG 20100427 MD GERMANY

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
6698963 1013578710 PS LAPATINIB 2 22059
6698963 1013578711 SS OXALIPLATIN 1
6698963 1013578712 SS FLUOROURACIL 1
6698963 1013578713 SS FOLINIC ACID 2
6698963 1013578714 C METOPROLOL 2 95MG TWICE PER DAY
6698963 1013578715 C RAMIPRIL 1 2.5MG AS REQUIRED
6698963 1013578716 C PREDNISOLONE 1 7MG PER DAY
6698963 1013578717 C CREON 1 25000MG SIX TIMES PER DAY
6698963 1013578718 C LOPERAMIDE 1 2MG AS REQUIRED
6698963 1013578719 C PANTOZOL 2 40MG PER DAY
6698963 1013578720 C ASPIRIN 1
6698963 1013578721 C LANTUS 1
6698963 1013578722 C ACTRAPID 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6698963 1013578714 HYPERTENSION
6698963 1013578715 HYPERTENSION
6698963 1013578716 RHEUMATOID ARTHRITIS
6698963 1013578717 PANCREATIC INSUFFICIENCY
6698963 1013578719 PROPHYLAXIS

Outcome of event

Event ID OUTC COD
6698963 HO

Reactions reported

Event ID PT
6698963 DYSARTHRIA
6698963 MUSCULAR WEAKNESS
6698963 TRANSIENT ISCHAEMIC ATTACK

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
6698963 1013578710 20100309
6698963 1013578711 20100224
6698963 1013578712 20100303
6698963 1013578713 20100303
6698963 1013578715 20090506
6698963 1013578716 20090325
6698963 1013578717 20090506
6698963 1013578718 20090715
6698963 1013578719 20090506