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

FLUSHING ( 255 FDA reports)
PRURITUS ( 74 FDA reports)
PARAESTHESIA ( 63 FDA reports)
DIZZINESS ( 61 FDA reports)
FATIGUE ( 57 FDA reports)
MYALGIA ( 57 FDA reports)
OEDEMA PERIPHERAL ( 57 FDA reports)
NAUSEA ( 55 FDA reports)
PAIN ( 54 FDA reports)
ARTHRALGIA ( 48 FDA reports)
HEADACHE ( 45 FDA reports)
ANXIETY ( 44 FDA reports)
CHEST PAIN ( 43 FDA reports)
DIARRHOEA ( 41 FDA reports)
FALL ( 41 FDA reports)
VOMITING ( 41 FDA reports)
MYOCARDIAL INFARCTION ( 40 FDA reports)
BLOOD GLUCOSE INCREASED ( 39 FDA reports)
ASTHENIA ( 37 FDA reports)
DYSPNOEA ( 36 FDA reports)
FEELING HOT ( 36 FDA reports)
PAIN IN EXTREMITY ( 36 FDA reports)
DRUG INEFFECTIVE ( 31 FDA reports)
INSOMNIA ( 31 FDA reports)
BACK PAIN ( 29 FDA reports)
RENAL FAILURE ACUTE ( 29 FDA reports)
ERYTHEMA ( 28 FDA reports)
RASH ( 28 FDA reports)
CONSTIPATION ( 27 FDA reports)
DEHYDRATION ( 27 FDA reports)
INJURY ( 27 FDA reports)
MUSCLE SPASMS ( 27 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 26 FDA reports)
CORONARY ARTERY DISEASE ( 25 FDA reports)
COUGH ( 25 FDA reports)
WEIGHT INCREASED ( 25 FDA reports)
ATRIAL FIBRILLATION ( 24 FDA reports)
HYPERTENSION ( 24 FDA reports)
DEPRESSION ( 23 FDA reports)
URINARY TRACT INFECTION ( 23 FDA reports)
ABDOMINAL PAIN UPPER ( 22 FDA reports)
HYPOAESTHESIA ( 22 FDA reports)
ANAEMIA ( 20 FDA reports)
ABDOMINAL PAIN ( 19 FDA reports)
LOSS OF CONSCIOUSNESS ( 19 FDA reports)
PNEUMONIA ( 19 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
ARRHYTHMIA ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 18 FDA reports)
CHILLS ( 18 FDA reports)
DYSPEPSIA ( 18 FDA reports)
FEAR ( 18 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 18 FDA reports)
OSTEOARTHRITIS ( 18 FDA reports)
PULMONARY HYPERTENSION ( 18 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 18 FDA reports)
BURNING SENSATION ( 17 FDA reports)
EMOTIONAL DISTRESS ( 17 FDA reports)
HOT FLUSH ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
UNEVALUABLE EVENT ( 17 FDA reports)
AMNESIA ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
GYNAECOMASTIA ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
SCAR ( 16 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 15 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 15 FDA reports)
MICTURITION URGENCY ( 15 FDA reports)
RHABDOMYOLYSIS ( 15 FDA reports)
ANHEDONIA ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 14 FDA reports)
DIABETES MELLITUS ( 14 FDA reports)
HEART RATE INCREASED ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
PAIN IN JAW ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
URTICARIA ( 14 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 13 FDA reports)
BONE DISORDER ( 13 FDA reports)
BONE PAIN ( 13 FDA reports)
MALAISE ( 13 FDA reports)
NEPHROLITHIASIS ( 13 FDA reports)
NOCTURIA ( 13 FDA reports)
RENAL INJURY ( 13 FDA reports)
SINUSITIS ( 13 FDA reports)
TREMOR ( 13 FDA reports)
URINARY INCONTINENCE ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
BLOOD UREA INCREASED ( 12 FDA reports)
CEREBRAL ATROPHY ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
DIVERTICULUM INTESTINAL ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
GLOSSODYNIA ( 12 FDA reports)
HERPES ZOSTER ( 12 FDA reports)
INFECTION ( 12 FDA reports)
LETHARGY ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 12 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 12 FDA reports)
SKIN BURNING SENSATION ( 12 FDA reports)
SWELLING ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
URINE ABNORMALITY ( 12 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 11 FDA reports)
BLISTER ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
BONE FORMATION INCREASED ( 11 FDA reports)
CARDIOVASCULAR DISORDER ( 11 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DILATATION ATRIAL ( 11 FDA reports)
DIVERTICULITIS ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 11 FDA reports)
LOOSE TOOTH ( 11 FDA reports)
MEMORY IMPAIRMENT ( 11 FDA reports)
NECK PAIN ( 11 FDA reports)
POLLAKIURIA ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
RHINITIS ALLERGIC ( 11 FDA reports)
TONGUE ULCERATION ( 11 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 10 FDA reports)
CARDIAC DISORDER ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 10 FDA reports)
JOINT SWELLING ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
NASAL CONGESTION ( 10 FDA reports)
NERVOUSNESS ( 10 FDA reports)
SLEEP DISORDER ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
AZOTAEMIA ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BREATH ODOUR ( 9 FDA reports)
CARDIAC OUTPUT DECREASED ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CONVULSION ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
ENDOTRACHEAL INTUBATION ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
MEDICATION RESIDUE ( 9 FDA reports)
MOUTH ULCERATION ( 9 FDA reports)
MULTIPLE INJURIES ( 9 FDA reports)
SEPTIC SHOCK ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
ABASIA ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ANGINA UNSTABLE ( 8 FDA reports)
BASAL GANGLIA INFARCTION ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CHROMATURIA ( 8 FDA reports)
COLONIC STENOSIS ( 8 FDA reports)
DEATH ( 8 FDA reports)
DENTAL CLEANING ( 8 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HIP FRACTURE ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
ILEUS ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 8 FDA reports)
SUBDURAL HAEMATOMA ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
ARTERIAL STENOSIS ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
ERECTILE DYSFUNCTION ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
HEPATOSPLENOMEGALY ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
LOCAL SWELLING ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OBESITY ( 6 FDA reports)
ORTHOPNOEA ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
STENT PLACEMENT ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
APATHY ( 5 FDA reports)
ARACHNOID CYST ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
DILATATION VENTRICULAR ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FAECES PALE ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GOUT ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
MASS ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
POLYP ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RETCHING ( 5 FDA reports)
SINUS CONGESTION ( 5 FDA reports)
SPLENOMEGALY ( 5 FDA reports)
SURGERY ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TOBACCO ABUSE ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
OESOPHAGEAL DILATATION ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
STRESS ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ULCER ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EDUCATIONAL PROBLEM ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BREAST CANCER MALE ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BUNION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CYST ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALLOPIAN TUBE CANCER METASTATIC ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONITIS CHEMICAL ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE DESQUAMATION ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
MISCARRIAGE OF PARTNER ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TENSION ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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