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

DYSPNOEA ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
FALL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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