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

NAUSEA ( 31 FDA reports)
DYSPNOEA ( 21 FDA reports)
HYPERTENSION ( 21 FDA reports)
DIZZINESS ( 20 FDA reports)
DRUG INEFFECTIVE ( 20 FDA reports)
FATIGUE ( 19 FDA reports)
VOMITING ( 18 FDA reports)
ASTHENIA ( 17 FDA reports)
HEADACHE ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
ANAEMIA ( 16 FDA reports)
FALL ( 16 FDA reports)
HYPOTENSION ( 16 FDA reports)
COMPLETED SUICIDE ( 15 FDA reports)
COUGH ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
ANXIETY ( 12 FDA reports)
ARTHRALGIA ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
RASH ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
MALAISE ( 9 FDA reports)
PAIN ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
AGITATION ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
MELAENA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
THROMBOSIS IN DEVICE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INJECTION SITE PAIN ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
POISONING ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TREMOR ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
REACTIVE PSYCHOSIS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEAR ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENTRICLE RUPTURE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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