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

CATARACT ( 5 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
TREMOR ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
ABASIA ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FALL ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
EXOSTOSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)

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