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
4542773 5693753 F 4542773-3 20041115 20041202 20041231 EXP 200413720JP AVENTIS PHARMACEUTICALS, INC. 75 YR F Y 47.5 KG 20041231 MD

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
4542773 1005546826 PS TAXOTERE 1 INTRAVENOUS DRIP
4542773 1005546827 C DECADRON 1 INTRAVENOUS DRIP
4542773 1005546828 C KYTRIL 1 INTRAVENOUS DRIP
4542773 1005546829 C GASMOTIN 2 ORAL
4542773 1005546830 C NITROL 1 ORAL
4542773 1005546831 C DILTIAZEM HCL 1 ORAL
4542773 1005546832 C ZANTAC 1 ORAL
4542773 1005546833 C ALDACTONE 1 ORAL
4542773 1005546834 C LONGES 2 ORAL
4542773 1005546835 C ASPIRIN 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
4542773 1005546826 CARCINOMA
4542773 1005546827 NAUSEA
4542773 1005546828 NAUSEA
4542773 1005546829 GASTRITIS
4542773 1005546830 MYOCARDIAL ISCHAEMIA
4542773 1005546831 MYOCARDIAL ISCHAEMIA
4542773 1005546832 GASTRIC ULCER
4542773 1005546833 CARDIAC FAILURE
4542773 1005546834 HYPERTENSION
4542773 1005546835 MYOCARDIAL ISCHAEMIA

Outcome of event

Event ID OUTC COD
4542773 HO

Reactions reported

Event ID PT
4542773 ANOREXIA
4542773 GASTRIC ULCER
4542773 GASTRITIS
4542773 OESOPHAGITIS

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

Event ID RPSR COD
4542773 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4542773 1005546826 20041104 20041111
4542773 1005546827 20041104 20041124
4542773 1005546828 20041104 20041124