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
5472368 6361941 F 5472368-9 20070628 20070921 20070930 EXP FR-SHR-FR-2007-026157 BERLEX 76 YR F Y 70 KG 20070928 MD FRANCE

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
5472368 1008989690 PS ULTRAVIST 300 1 INTRAVENOUS 130 ML, 1 DOSE 64517E 020220
5472368 1008989691 C AMARYL 1 ORAL 4 MG, 1X/DAY
5472368 1008989692 C PHYSIOTENS ^GIULINI^ 2 ORAL .4 UNK, 1X/DAY
5472368 1008989693 C GLUCOPHAGE 1 ORAL 2000 MG, 1X/DAY
5472368 1008989694 C ACTOS 1 ORAL 1 TAB(S), 1X/DAY
5472368 1008989695 C SKENAN 2 ORAL 2 CAP(S), 1X/DAY
5472368 1008989696 C VERAPAMIL 1 ORAL 240 MG, 2X/DAY
5472368 1008989697 C KARDEGIC /FRA/ 2 ORAL 1 TAB(S), 1X/DAY
5472368 1008989698 C LISINOPRIL 1 ORAL 1 TAB(S), 1X/DAY
5472368 1008989699 C TRANXENE 1 ORAL 1 TAB(S), 1X/DAY
5472368 1008989700 C OMEPRAZOLE 1 ORAL 1 TAB(S), 1X/6 WEEKS
5472368 1008989701 C FOSAMAX 1 ORAL 1 TAB(S), 1X/DAY
5472368 1008989702 C ESCITALOPRAM OXALATE 1 ORAL 1 TAB(S), 1X/DAY
5472368 1008989703 C FUMAFER 2 ORAL 2 TAB(S), 1X/DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
5472368 1008989691 TYPE 2 DIABETES MELLITUS
5472368 1008989693 TYPE 2 DIABETES MELLITUS
5472368 1008989694 TYPE 2 DIABETES MELLITUS
5472368 1008989695 PAIN

Outcome of event

Event ID OUTC COD
5472368 HO

Reactions reported

Event ID PT
5472368 ACUTE PULMONARY OEDEMA
5472368 CYANOSIS
5472368 DYSPNOEA
5472368 MALAISE

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
5472368 1008989690 20070628 20070628