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
5903218 6403179 F 5903218-1 20080926 20080930 EXP A0675309A GLAXOSMITHKLINE 58 YR F Y 20080930 CN 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
5903218 1010519799 PS ALLI 1 ORAL UNK 021887

Indications of drugs used

Event ID DRUG SEQ INDI PT
5903218 1010519799 WEIGHT LOSS DIET

Outcome of event

Event ID OUTC COD
5903218 OT

Reactions reported

Event ID PT
5903218 ABDOMINAL PAIN UPPER
5903218 ASTHMA
5903218 BACK DISORDER
5903218 BACK PAIN
5903218 DIZZINESS
5903218 DRUG INEFFECTIVE
5903218 DYSPNOEA
5903218 FATIGUE
5903218 FEELING ABNORMAL
5903218 FLATULENCE
5903218 FOOD CRAVING
5903218 FRUSTRATION
5903218 GASTRIC DISORDER
5903218 GASTROENTERITIS VIRAL
5903218 GASTROINTESTINAL DISORDER
5903218 HYPERPHAGIA
5903218 INITIAL INSOMNIA
5903218 INSOMNIA
5903218 IRRITABLE BOWEL SYNDROME
5903218 LUNG DISORDER
5903218 MALAISE
5903218 MIGRAINE
5903218 MULTIPLE ALLERGIES
5903218 MUSCLE SPASMS
5903218 MUSCLE TIGHTNESS
5903218 MUSCULOSKELETAL STIFFNESS
5903218 MYALGIA
5903218 NASOPHARYNGITIS
5903218 NOCTURIA
5903218 OEDEMA PERIPHERAL
5903218 PAIN IN EXTREMITY
5903218 POLLAKIURIA
5903218 POOR QUALITY SLEEP
5903218 RECTAL DISCHARGE
5903218 SLEEP DISORDER
5903218 SNEEZING
5903218 STEATORRHOEA
5903218 STOMACH DISCOMFORT
5903218 STRESS
5903218 THERAPEUTIC RESPONSE UNEXPECTED
5903218 WEIGHT FLUCTUATION
5903218 WEIGHT INCREASED

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
5903218 1010519799 20070616