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

CEREBROVASCULAR ACCIDENT ( 34 FDA reports)
VOMITING ( 24 FDA reports)
NAUSEA ( 19 FDA reports)
DIARRHOEA ( 17 FDA reports)
DRUG INTERACTION ( 15 FDA reports)
DIZZINESS ( 13 FDA reports)
RASH ( 13 FDA reports)
CONVULSION ( 11 FDA reports)
MYALGIA ( 11 FDA reports)
TENDON RUPTURE ( 11 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
GOUTY ARTHRITIS ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
FALL ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
APHASIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
INJURY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
PANOPHTHALMITIS ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEATH ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSOPHOBIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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