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
8480331 8644634 I 8480331-9 20120301 20120620 20120630 EXP FR-TEVA-337839ISR TEVA 40 YR M Y 20120630 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
8480331 1020135241 C XANAX 0.5 MG, SCORED TABLET 2 ORAL 2 MILLIGRAM;
8480331 1020135240 C AERIUS 5 MG, COATED TABLET 2 5 MILLIGRAM;
8480331 1020135236 PS CIMETIDINE 1 ORAL 600 MILLIGRAM; 074151
8480331 1020135237 SS CIMETIDINE 1 ORAL 1000 MILLIGRAM; 074151
8480331 1020135242 C OROPERIDYS 2 ORAL 3 DOSAGE FORMS;
8480331 1020135238 C TAREG 80 MG, COATED SCORED TABLET 2 ORAL 80 MILLIGRAM;
8480331 1020135239 C MONO-TILDIEM 200 MG, CAPSULE 2 ORAL 200 MILLIGRAM;

Indications of drugs used

Event ID DRUG SEQ INDI PT
8480331 1020135236 PEPTIC ULCER
8480331 1020135238 HYPERTENSION
8480331 1020135239 HYPERTENSION

Outcome of event

Event ID OUTC COD
8480331 OT

Reactions reported

Event ID PT
8480331 URINARY TRACT INFECTION
8480331 ABDOMINAL DISTENSION
8480331 WEIGHT DECREASED
8480331 ASTHENIA
8480331 WHITE BLOOD CELL COUNT INCREASED
8480331 C-REACTIVE PROTEIN INCREASED
8480331 DECREASED APPETITE
8480331 ERECTILE DYSFUNCTION
8480331 GASTROOESOPHAGEAL REFLUX DISEASE

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
8480331 1020135236 20111129 20120301 4 MON
8480331 1020135237 20120301 4 MON