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
4463186 4158126 F 4463186-9 20040201 20040611 20040930 EXP US-ROCHE-371033 ROCHE 35 YR M Y 68 KG 20040930 CN

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
4463186 1005252462 PS PEGASYS 1 OTHER ROUTE REPORTED AS INJ. DOSE REPORTED AS 180/0.5 ML ONCE A WEEK. B0030
4463186 1005252463 SS COPEGUS 1 ORAL U3077
4463186 1005252464 SS COPEGUS 1 ORAL U3077

Indications of drugs used

Event ID DRUG SEQ INDI PT
4463186 1005252462 HEPATITIS C
4463186 1005252463 HEPATITIS C

Outcome of event

Event ID OUTC COD
4463186 OT

Reactions reported

Event ID PT
4463186 ANOREXIA
4463186 BLOOD BLISTER
4463186 BLOOD GLUCOSE INCREASED
4463186 BLOOD TRIGLYCERIDES INCREASED
4463186 CHEST PAIN
4463186 DEAFNESS
4463186 DIZZINESS
4463186 DRY SKIN
4463186 DYSPNOEA
4463186 FATIGUE
4463186 FORMICATION
4463186 GASTROOESOPHAGEAL REFLUX DISEASE
4463186 HAEMOGLOBIN DECREASED
4463186 HEADACHE
4463186 HEARING IMPAIRED
4463186 HOT FLUSH
4463186 HYPOTRICHOSIS
4463186 INSOMNIA
4463186 IRRITABILITY
4463186 MEMORY IMPAIRMENT
4463186 MOUTH ULCERATION
4463186 NAUSEA
4463186 PAIN
4463186 PRURITUS
4463186 RASH
4463186 SINUS CONGESTION
4463186 SINUS DISORDER
4463186 TONSILLITIS

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

Event ID RPSR COD
4463186 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4463186 1005252462 20040215 20040818
4463186 1005252463 20040215 20040818
4463186 1005252464 20040818