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
7488061 7398999 F 7488061-7 20011016 20110510 20110518 EXP US-ROCHE-622194 ROCHE 27 YR F Y 20110518 LW UNITED STATES

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
7488061 1016528133 PS ACCUTANE 1 UNKNOWN 018662
7488061 1016528134 SS SOTRET 1 ORAL
7488061 1016528135 C ORTHO TRI-CYCLEN 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
7488061 OT

Reactions reported

Event ID PT
7488061 ABDOMINAL ADHESIONS
7488061 BLOOD CHOLESTEROL INCREASED
7488061 INFLAMMATORY BOWEL DISEASE
7488061 DRY SKIN
7488061 HAEMOGLOBIN DECREASED
7488061 DEPRESSION
7488061 PELVIC ADHESIONS
7488061 LIP BLISTER
7488061 LIP DRY
7488061 RASH PAPULAR
7488061 COLITIS ULCERATIVE
7488061 URINARY TRACT INFECTION
7488061 STRESS
7488061 PROCTITIS
7488061 HAEMATOCRIT DECREASED
7488061 RED BLOOD CELL COUNT DECREASED
7488061 XEROSIS
7488061 ENDOMETRIOSIS
7488061 CROHN'S DISEASE
7488061 GASTROOESOPHAGEAL REFLUX DISEASE
7488061 SLEEP APNOEA SYNDROME

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
7488061 1016528133 20010911 20020201
7488061 1016528134 20070501 20070901