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

DYSPNOEA ( 42 FDA reports)
NAUSEA ( 34 FDA reports)
PYREXIA ( 34 FDA reports)
VOMITING ( 27 FDA reports)
COUGH ( 26 FDA reports)
INTERSTITIAL LUNG DISEASE ( 25 FDA reports)
MALAISE ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
ASTHMA ( 23 FDA reports)
PAIN ( 23 FDA reports)
ABDOMINAL PAIN ( 22 FDA reports)
CHEST DISCOMFORT ( 22 FDA reports)
DIZZINESS ( 22 FDA reports)
FATIGUE ( 22 FDA reports)
HEADACHE ( 22 FDA reports)
ANXIETY ( 19 FDA reports)
INSOMNIA ( 19 FDA reports)
ANAEMIA ( 18 FDA reports)
PNEUMONIA ( 18 FDA reports)
PRODUCTIVE COUGH ( 18 FDA reports)
CONSTIPATION ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
ERYTHEMA ( 17 FDA reports)
INFECTION ( 17 FDA reports)
PARAESTHESIA ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
CATARACT ( 15 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 15 FDA reports)
MUSCLE SPASMS ( 15 FDA reports)
WEIGHT INCREASED ( 15 FDA reports)
ARTHRALGIA ( 14 FDA reports)
DIABETES MELLITUS ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 13 FDA reports)
OROPHARYNGEAL PAIN ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
ACUTE SINUSITIS ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
DENTAL CARIES ( 11 FDA reports)
EXOSTOSIS ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
VISION BLURRED ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
ATELECTASIS ( 10 FDA reports)
BRONCHIECTASIS ( 10 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
DIVERTICULUM ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
MYOCARDIAL ISCHAEMIA ( 10 FDA reports)
OSTEONECROSIS OF JAW ( 10 FDA reports)
PRESYNCOPE ( 10 FDA reports)
RESTLESS LEGS SYNDROME ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
TOOTHACHE ( 10 FDA reports)
UPPER LIMB FRACTURE ( 10 FDA reports)
AGITATION ( 9 FDA reports)
AORTIC CALCIFICATION ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
BREAST CANCER ( 9 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 9 FDA reports)
DEFORMITY ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
EMPHYSEMA ( 9 FDA reports)
FACET JOINT SYNDROME ( 9 FDA reports)
FALL ( 9 FDA reports)
FIBROSIS ( 9 FDA reports)
IRITIS ( 9 FDA reports)
LUNG HYPERINFLATION ( 9 FDA reports)
MACULAR HOLE ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
OSTEOMYELITIS ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
RETINITIS ( 9 FDA reports)
SPUTUM PURULENT ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
TREMOR ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
BLOOD GLUCOSE DECREASED ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
RASH ( 8 FDA reports)
ROAD TRAFFIC ACCIDENT ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
CHILLS ( 7 FDA reports)
DEATH ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
DYSLALIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOKINESIA ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
SNORING ( 7 FDA reports)
VENOUS THROMBOSIS ( 7 FDA reports)
VENTRICULAR ARRHYTHMIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MUCOSAL HAEMORRHAGE ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
APHONIA ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
EAR INFECTION ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 5 FDA reports)
INGUINAL HERNIA ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NASAL DRYNESS ( 5 FDA reports)
PHARYNGEAL INFLAMMATION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
SCAR ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
EDUCATIONAL PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GALACTORRHOEA ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
LARYNGEAL ULCERATION ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGEAL INJURY ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANDROGENS ABNORMAL ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BIOPSY VAGINA ABNORMAL ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CNS GERMINOMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARASITE STOOL TEST ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 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)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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