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

CHOLELITHIASIS ( 15 FDA reports)
VOMITING ( 15 FDA reports)
NAUSEA ( 14 FDA reports)
PAIN ( 14 FDA reports)
CHEST PAIN ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
CHOLECYSTITIS CHRONIC ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
DYSPNOEA ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
OESOPHAGITIS ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
LOWER LIMB FRACTURE ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
GALLBLADDER DISORDER ( 8 FDA reports)
INJURY ( 8 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 8 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
SINUS ARRHYTHMIA ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
FALL ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
MELAENA ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RASH ( 6 FDA reports)
SPINAL LAMINECTOMY ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
MALAISE ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OSTEOGENESIS IMPERFECTA ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PROCEDURAL DIZZINESS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RADICULITIS CERVICAL ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MASS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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