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

RHABDOMYOLYSIS ( 18 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
NAUSEA ( 13 FDA reports)
DIARRHOEA ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
FALL ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
GASTROENTERITIS VIRAL ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
RASH ( 9 FDA reports)
CELLULITIS ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ANURIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RENAL ARTERY THROMBOSIS ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
FEAR ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
LOSS OF LIBIDO ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
PAIN ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COLITIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEILITIS GRANULOMATOSA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MELKERSSON-ROSENTHAL SYNDROME ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VENOUS PRESSURE JUGULAR DECREASED ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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