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

EYE IRRITATION ( 35 FDA reports)
PYREXIA ( 35 FDA reports)
EYE PAIN ( 33 FDA reports)
FATIGUE ( 33 FDA reports)
VOMITING ( 30 FDA reports)
ANAEMIA ( 29 FDA reports)
PNEUMONIA ( 29 FDA reports)
ANXIETY ( 28 FDA reports)
KERATITIS ( 27 FDA reports)
VISUAL ACUITY REDUCED ( 27 FDA reports)
DYSPNOEA ( 26 FDA reports)
HYPOTENSION ( 26 FDA reports)
ASTHENIA ( 25 FDA reports)
CHEST PAIN ( 25 FDA reports)
HEADACHE ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
PAIN ( 25 FDA reports)
MALAISE ( 24 FDA reports)
NAUSEA ( 24 FDA reports)
DEPRESSION ( 23 FDA reports)
DIZZINESS ( 23 FDA reports)
SEPSIS ( 23 FDA reports)
FALL ( 22 FDA reports)
BACK PAIN ( 21 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
CONSTIPATION ( 19 FDA reports)
EYE OPERATION COMPLICATION ( 19 FDA reports)
RASH ( 19 FDA reports)
ATRIAL FIBRILLATION ( 18 FDA reports)
SINUSITIS ( 18 FDA reports)
SYNCOPE ( 18 FDA reports)
ARTHRALGIA ( 17 FDA reports)
CHILLS ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
DIARRHOEA ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
HYPERTENSION ( 17 FDA reports)
OCULAR HYPERAEMIA ( 17 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
INSOMNIA ( 15 FDA reports)
URINARY TRACT INFECTION ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
WEIGHT DECREASED ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
DRY MOUTH ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
DEHYDRATION ( 13 FDA reports)
DRY EYE ( 13 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
SLEEP DISORDER ( 13 FDA reports)
BLINDNESS ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
DEATH ( 12 FDA reports)
IMPAIRED HEALING ( 12 FDA reports)
LACRIMATION INCREASED ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
RHEUMATOID ARTHRITIS ( 12 FDA reports)
EMOTIONAL DISTRESS ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
LYMPHADENOPATHY ( 11 FDA reports)
RENAL FAILURE ( 11 FDA reports)
SPINAL OSTEOARTHRITIS ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
DIVERTICULITIS ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
MUSCULOSKELETAL PAIN ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
PHOTOPHOBIA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
COAGULOPATHY ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
DYSPEPSIA ( 9 FDA reports)
EYE PRURITUS ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
OSTEOARTHRITIS ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
SINUS CONGESTION ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
INFECTION ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
OESOPHAGITIS ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SCOLIOSIS ( 8 FDA reports)
ATELECTASIS ( 7 FDA reports)
CATARACT ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
CORNEAL DISORDER ( 7 FDA reports)
CORNEAL OEDEMA ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
EYE MOVEMENT DISORDER ( 7 FDA reports)
EYE SWELLING ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
GINGIVAL DISORDER ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
METASTASES TO SPINE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OSTEOSCLEROSIS ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
SNORING ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BONE LESION ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
COLITIS ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
FAT NECROSIS ( 6 FDA reports)
FEAR ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
ORAL INFECTION ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PERIODONTAL DISEASE ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
TOOTH FRACTURE ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
VITAMIN D DECREASED ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ALVEOLITIS ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
EXPOSED BONE IN JAW ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
FAILURE TO THRIVE ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANGER ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BENIGN BONE NEOPLASM ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CAECITIS ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CHEMICAL BURNS OF EYE ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
CYSTITIS RADIATION ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STRESS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
BURSITIS INFECTIVE ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 3 FDA reports)
CONTACT LENS INTOLERANCE ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EAGLE BARRETT SYNDROME ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GIANT PAPILLARY CONJUNCTIVITIS ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MONONUCLEOSIS SYNDROME ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OCULAR TOXICITY ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OSTEOPETROSIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY HYPOPLASIA ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL DYSPLASIA ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TALIPES ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VITREOUS DETACHMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL INFILTRATES ( 2 FDA reports)
CORNEAL STRIAE ( 2 FDA reports)
CORNEAL THINNING ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
KERATITIS BACTERIAL ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
PULMONARY CALCIFICATION ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITREOUS DEGENERATION ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CORNEAL CYST ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL STAINING ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DACRYOLITH ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS ATROPHY ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKIN WOUND ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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