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

FATIGUE ( 43 FDA reports)
PYREXIA ( 43 FDA reports)
NAUSEA ( 28 FDA reports)
DIARRHOEA ( 23 FDA reports)
DIZZINESS ( 23 FDA reports)
DYSPNOEA ( 23 FDA reports)
OSTEONECROSIS ( 23 FDA reports)
PNEUMONIA ( 22 FDA reports)
VOMITING ( 22 FDA reports)
SEPSIS ( 21 FDA reports)
HYPOTENSION ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
CEREBRAL INFARCTION ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
MUSCULAR WEAKNESS ( 14 FDA reports)
TRANSAMINASES INCREASED ( 14 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
FALL ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
RENAL FAILURE ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
VISION BLURRED ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ARTHRALGIA ( 9 FDA reports)
CONVULSION ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SWELLING ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
DEATH ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
PAIN ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
PULMONARY FIBROSIS ( 8 FDA reports)
RASH ( 8 FDA reports)
RENAL TUBULAR NECROSIS ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
COLITIS ( 7 FDA reports)
COUGH ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
TREMOR ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
AGEUSIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
APATHY ( 5 FDA reports)
APHASIA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COLECTOMY ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
UTERINE ATONY ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
POOR PERSONAL HYGIENE ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RECTAL OBSTRUCTION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACETONAEMIA ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BENIGN RESPIRATORY TRACT NEOPLASM ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GOUT ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORAL VIRAL INFECTION ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHISTOSOMIASIS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TULARAEMIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR DRAINAGE ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VON WILLEBRAND'S FACTOR ANTIGEN INCREASED ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)

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