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
8016630 8312348 F 8016630-4 20111209 20111226 20111231 EXP PHHY2011GB111714 SANDOZ,INC. 54 YR M Y 20111231 OT 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
8016630 1018419922 C OTHER THERAPEUTIC PRODUCTS/AZD6140/PLACEBO 2 ORAL UNK
8016630 1018419920 PS METFORMIN HCL 1 ORAL UNK 075985
8016630 1018419924 C ATORVASTATIN 1 UNK
8016630 1018419925 C BISOPROLOL 2 UNK
8016630 1018419921 SS RAMIPRIL 1 ORAL UNK UKN, UNK
8016630 1018419923 C ACETYLSALICYLIC ACID SRT 1 ORAL 75 MG, QD
8016630 1018419926 C FUROSEMIDE 1 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8016630 1018419922 CORONARY ARTERY DISEASE
8016630 1018419920 DIABETES MELLITUS
8016630 1018419924 HYPERCHOLESTEROLAEMIA
8016630 1018419925 HYPERTENSION
8016630 1018419921 HYPERTENSION
8016630 1018419926 HYPERTENSION

Outcome of event

Event ID OUTC COD
8016630 HO
8016630 LT
8016630 OT

Reactions reported

Event ID PT
8016630 RENAL FAILURE ACUTE
8016630 HYPOTHERMIA
8016630 MALAISE
8016630 SEPSIS
8016630 VOMITING
8016630 CIRCULATORY COLLAPSE
8016630 HYPOGLYCAEMIA

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
8016630 1018419922 20111117 20111209 23 DAY