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

DRUG INTERACTION ( 33 FDA reports)
DYSPNOEA ( 33 FDA reports)
PYREXIA ( 29 FDA reports)
RENAL FAILURE ( 28 FDA reports)
VOMITING ( 25 FDA reports)
PULMONARY EMBOLISM ( 24 FDA reports)
BRONCHOPNEUMONIA ( 22 FDA reports)
RASH ( 21 FDA reports)
ASTHENIA ( 20 FDA reports)
PNEUMONIA ( 19 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 19 FDA reports)
SEPSIS ( 17 FDA reports)
DEATH ( 16 FDA reports)
COUGH ( 15 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 15 FDA reports)
STEVENS-JOHNSON SYNDROME ( 15 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
HEPATIC FAILURE ( 14 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
HAEMOLYTIC ANAEMIA ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
CEREBRAL HAEMORRHAGE ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
ILEUS PARALYTIC ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
CARDIOPULMONARY FAILURE ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
FALL ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
BLISTER ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
MALAISE ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 9 FDA reports)
CONVULSION ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
HYPERTENSIVE CRISIS ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
SEPTIC SHOCK ( 9 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
ELECTROLYTE IMBALANCE ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
NIKOLSKY'S SIGN ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PETECHIAE ( 8 FDA reports)
PILONIDAL CYST CONGENITAL ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
CHILLS ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FLAT FEET ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 7 FDA reports)
PYOTHORAX ( 7 FDA reports)
SPINAL DISORDER ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
TREMOR ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
AGITATION ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
QUADRIPLEGIA ( 5 FDA reports)
SHOCK ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRY GANGRENE ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TALIPES ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRUSH SYNDROME ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLUCAGONOMA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOURICAEMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOWER MOTOR NEURONE LESION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYURIA ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION COMPLETE ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BITE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CLUTTERING ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIV INFECTION CDC CATEGORY C3 ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODULE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOLOSA-HUNT SYNDROME ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC SPINAL CORD COMPRESSION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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