Please choose an event type to view the corresponding MedsFacts report:

DEPRESSION ( 23 FDA reports)
DRY EYE ( 23 FDA reports)
FOLLICULITIS ( 23 FDA reports)
VOMITING ( 23 FDA reports)
BRONCHITIS ( 18 FDA reports)
ECZEMA ( 15 FDA reports)
PNEUMONIA ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
ASTEATOSIS ( 13 FDA reports)
BACK PAIN ( 13 FDA reports)
CHEILITIS ( 13 FDA reports)
COLITIS ( 13 FDA reports)
COLITIS ULCERATIVE ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
EPISTAXIS ( 13 FDA reports)
HAEMANGIOMA ( 13 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 13 FDA reports)
LIP DRY ( 13 FDA reports)
OCULAR HYPERAEMIA ( 13 FDA reports)
PEPTIC ULCER ( 13 FDA reports)
PLEURISY ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
TREMOR ( 13 FDA reports)
VISUAL ACUITY REDUCED ( 13 FDA reports)
ARTHRALGIA ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
ONYCHOMYCOSIS ( 11 FDA reports)
APATHY ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 10 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
EYE PAIN ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HERPES ZOSTER ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
HYPERLIPIDAEMIA ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
MULTIPLE MYELOMA ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
PAIN ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SEBORRHOEIC DERMATITIS ( 10 FDA reports)
SLEEP DISORDER ( 10 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 10 FDA reports)
STOMATITIS ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
VITREOUS FLOATERS ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
ARTHROSCOPY ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
BONE MARROW TRANSPLANT ( 9 FDA reports)
CATARACT ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DRY SKIN ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
EYE LASER SURGERY ( 9 FDA reports)
EYELID MARGIN CRUSTING ( 9 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 9 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 9 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 9 FDA reports)
OBESITY ( 9 FDA reports)
PLASMACYTOMA ( 9 FDA reports)
POLYDIPSIA ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
RASH ( 9 FDA reports)
ROSACEA ( 9 FDA reports)
STEM CELL TRANSPLANT ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
ARTHRITIS ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
COSTOCHONDRITIS ( 8 FDA reports)
COUGH ( 8 FDA reports)
GASTROENTERITIS VIRAL ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
VIRAL PHARYNGITIS ( 8 FDA reports)
ASTIGMATISM ( 7 FDA reports)
DERMATITIS ATOPIC ( 7 FDA reports)
HYPERMETROPIA ( 7 FDA reports)
PRESBYOPIA ( 7 FDA reports)
PROCTITIS ( 7 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
CLOSTRIDIUM TEST ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)

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