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

HYPERTENSION ( 33 FDA reports)
FALL ( 32 FDA reports)
HAEMORRHAGIC STROKE ( 24 FDA reports)
COLD SWEAT ( 23 FDA reports)
MALAISE ( 23 FDA reports)
INSOMNIA ( 19 FDA reports)
BRAIN DEATH ( 16 FDA reports)
COAGULOPATHY ( 16 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
ECONOMIC PROBLEM ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
ABNORMAL BEHAVIOUR ( 13 FDA reports)
DIZZINESS ( 13 FDA reports)
DYSPNOEA ( 13 FDA reports)
ACUTE RESPIRATORY FAILURE ( 12 FDA reports)
ANEURYSM ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
MULTIPLE INJURIES ( 11 FDA reports)
APNOEA ( 10 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
VOMITING ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
PAIN ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
ASTHMA ( 8 FDA reports)
BRAIN INJURY ( 8 FDA reports)
COUGH ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DERMAL CYST ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DIABETIC NEPHROPATHY ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
RASH ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CAROTID ARTERY STENOSIS ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPERTENSIVE HEART DISEASE ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
LOBAR PNEUMONIA ( 5 FDA reports)
MANIA ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
TOBACCO USER ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INJURY ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEAR ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MODERATE MENTAL RETARDATION ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ONYCHOGRYPHOSIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

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