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

PYREXIA ( 170 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 122 FDA reports)
MALAISE ( 105 FDA reports)
PLATELET COUNT DECREASED ( 104 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 99 FDA reports)
INTERSTITIAL LUNG DISEASE ( 94 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 93 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 86 FDA reports)
PNEUMONIA ( 85 FDA reports)
ANAEMIA ( 78 FDA reports)
LIVER DISORDER ( 78 FDA reports)
RASH ( 75 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 73 FDA reports)
DECREASED APPETITE ( 71 FDA reports)
DIARRHOEA ( 71 FDA reports)
LOSS OF CONSCIOUSNESS ( 68 FDA reports)
NAUSEA ( 64 FDA reports)
PLEURAL EFFUSION ( 58 FDA reports)
DIZZINESS ( 56 FDA reports)
VOMITING ( 56 FDA reports)
HAEMOGLOBIN DECREASED ( 55 FDA reports)
FALL ( 54 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 53 FDA reports)
INSOMNIA ( 49 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 49 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 48 FDA reports)
SEPSIS ( 48 FDA reports)
CONVULSION ( 46 FDA reports)
RHABDOMYOLYSIS ( 46 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 45 FDA reports)
HYPONATRAEMIA ( 45 FDA reports)
RENAL FAILURE ACUTE ( 43 FDA reports)
STEVENS-JOHNSON SYNDROME ( 43 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 41 FDA reports)
IRRITABILITY ( 41 FDA reports)
NEUTROPHIL COUNT DECREASED ( 41 FDA reports)
RESPIRATORY FAILURE ( 41 FDA reports)
DELIRIUM ( 40 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 39 FDA reports)
DYSPNOEA ( 39 FDA reports)
HYPERTENSION ( 37 FDA reports)
MUSCULAR WEAKNESS ( 37 FDA reports)
OVERDOSE ( 37 FDA reports)
CARDIAC ARREST ( 36 FDA reports)
CEREBRAL INFARCTION ( 36 FDA reports)
GAIT DISTURBANCE ( 36 FDA reports)
PNEUMONIA ASPIRATION ( 35 FDA reports)
RENAL IMPAIRMENT ( 35 FDA reports)
ASCITES ( 33 FDA reports)
BLOOD CREATININE INCREASED ( 33 FDA reports)
SOMNOLENCE ( 33 FDA reports)
THROMBOCYTOPENIA ( 33 FDA reports)
CARDIAC FAILURE ( 32 FDA reports)
HYPOAESTHESIA ( 32 FDA reports)
SUICIDE ATTEMPT ( 32 FDA reports)
DRUG INTERACTION ( 31 FDA reports)
HEADACHE ( 31 FDA reports)
DEATH ( 30 FDA reports)
ERYTHEMA ( 30 FDA reports)
ANOREXIA ( 29 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 29 FDA reports)
HALLUCINATION ( 29 FDA reports)
STOMATITIS ( 29 FDA reports)
ASTHENIA ( 28 FDA reports)
NEUTROPENIA ( 28 FDA reports)
AGRANULOCYTOSIS ( 27 FDA reports)
BLOOD PRESSURE DECREASED ( 27 FDA reports)
BLOOD UREA INCREASED ( 27 FDA reports)
CARDIO-RESPIRATORY ARREST ( 27 FDA reports)
CONSTIPATION ( 27 FDA reports)
DISEASE PROGRESSION ( 27 FDA reports)
CONDITION AGGRAVATED ( 26 FDA reports)
DYSPHAGIA ( 26 FDA reports)
HYPOGLYCAEMIA ( 26 FDA reports)
LEUKOPENIA ( 26 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 25 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
HYPERGLYCAEMIA ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
AGGRESSION ( 24 FDA reports)
ALOPECIA ( 24 FDA reports)
ANGINA PECTORIS ( 24 FDA reports)
BLOOD BILIRUBIN INCREASED ( 24 FDA reports)
COMA ( 24 FDA reports)
GASTRIC ULCER ( 24 FDA reports)
INTENTIONAL OVERDOSE ( 24 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 24 FDA reports)
OEDEMA ( 24 FDA reports)
TREMOR ( 24 FDA reports)
FEBRILE NEUTROPENIA ( 23 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 23 FDA reports)
SHOCK ( 23 FDA reports)
SUICIDAL IDEATION ( 23 FDA reports)
COMPLETED SUICIDE ( 22 FDA reports)
DRUG ERUPTION ( 22 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 22 FDA reports)
RENAL DISORDER ( 22 FDA reports)
ANXIETY ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 21 FDA reports)
BLOOD SODIUM DECREASED ( 21 FDA reports)
DYSKINESIA ( 21 FDA reports)
FATIGUE ( 21 FDA reports)
MULTI-ORGAN FAILURE ( 21 FDA reports)
PRURITUS ( 21 FDA reports)
RESPIRATORY ARREST ( 21 FDA reports)
DEHYDRATION ( 20 FDA reports)
HYPOALBUMINAEMIA ( 20 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 20 FDA reports)
AGITATION ( 19 FDA reports)
BONE MARROW FAILURE ( 19 FDA reports)
ENCEPHALOPATHY ( 19 FDA reports)
JAUNDICE ( 19 FDA reports)
OFF LABEL USE ( 19 FDA reports)
STAPHYLOCOCCAL INFECTION ( 19 FDA reports)
URINARY TRACT INFECTION ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 18 FDA reports)
HEPATIC ENCEPHALOPATHY ( 18 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 18 FDA reports)
PULMONARY EMBOLISM ( 18 FDA reports)
VENTRICULAR TACHYCARDIA ( 18 FDA reports)
ABDOMINAL PAIN UPPER ( 17 FDA reports)
ABNORMAL BEHAVIOUR ( 17 FDA reports)
BRADYCARDIA ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 17 FDA reports)
NASOPHARYNGITIS ( 17 FDA reports)
BLOOD ALBUMIN DECREASED ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
CONTUSION ( 16 FDA reports)
DELUSION ( 16 FDA reports)
DEPRESSION ( 16 FDA reports)
FEELING ABNORMAL ( 16 FDA reports)
HYPERHIDROSIS ( 16 FDA reports)
HYPOTHYROIDISM ( 16 FDA reports)
RENAL CELL CARCINOMA ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
BACK PAIN ( 15 FDA reports)
BLOOD AMYLASE INCREASED ( 15 FDA reports)
BLOOD POTASSIUM INCREASED ( 15 FDA reports)
CELLULITIS ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
COUGH ( 15 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
ILEUS ( 15 FDA reports)
MELAENA ( 15 FDA reports)
PANCYTOPENIA ( 15 FDA reports)
SEROTONIN SYNDROME ( 15 FDA reports)
SUDDEN DEATH ( 15 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
DYSARTHRIA ( 14 FDA reports)
HAEMATOCRIT DECREASED ( 14 FDA reports)
HYPERKALAEMIA ( 14 FDA reports)
LIPASE INCREASED ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
ABDOMINAL DISCOMFORT ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
HYPOKALAEMIA ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
NEPHROTIC SYNDROME ( 13 FDA reports)
NEUROPATHY PERIPHERAL ( 13 FDA reports)
PLEURISY ( 13 FDA reports)
PROTEIN TOTAL DECREASED ( 13 FDA reports)
PURPURA ( 13 FDA reports)
RESPIRATORY DEPRESSION ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
AMNESIA ( 12 FDA reports)
BLISTER ( 12 FDA reports)
DYSURIA ( 12 FDA reports)
GENERALISED OEDEMA ( 12 FDA reports)
INTESTINAL OBSTRUCTION ( 12 FDA reports)
MANIA ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 11 FDA reports)
ENTEROCOLITIS ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
GENERALISED ERYTHEMA ( 11 FDA reports)
HERPES ZOSTER ( 11 FDA reports)
HYPERLIPIDAEMIA ( 11 FDA reports)
HYPOGLYCAEMIC COMA ( 11 FDA reports)
HYPOTENSION ( 11 FDA reports)
HYPOXIA ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
OSTEOMYELITIS ( 11 FDA reports)
OXYGEN SATURATION DECREASED ( 11 FDA reports)
PARKINSONISM ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
SPEECH DISORDER ( 11 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 10 FDA reports)
DECUBITUS ULCER ( 10 FDA reports)
EPILEPSY ( 10 FDA reports)
EPISTAXIS ( 10 FDA reports)
GRAFT THROMBOSIS ( 10 FDA reports)
GRANULOCYTOPENIA ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
LIMB OPERATION ( 10 FDA reports)
LUNG NEOPLASM MALIGNANT ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
PERSECUTORY DELUSION ( 10 FDA reports)
PSYCHIATRIC SYMPTOM ( 10 FDA reports)
PYELONEPHRITIS ( 10 FDA reports)
RASH GENERALISED ( 10 FDA reports)
SCHIZOPHRENIA ( 10 FDA reports)
SEDATION ( 10 FDA reports)
TOE AMPUTATION ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
DRY SKIN ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
GASTROINTESTINAL PERFORATION ( 9 FDA reports)
HAEMATEMESIS ( 9 FDA reports)
HALLUCINATION, AUDITORY ( 9 FDA reports)
HALLUCINATION, VISUAL ( 9 FDA reports)
HEMIPLEGIA ( 9 FDA reports)
HYPOCALCAEMIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
IRON DEFICIENCY ANAEMIA ( 9 FDA reports)
METASTASES TO LYMPH NODES ( 9 FDA reports)
MOVEMENT DISORDER ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
RESTLESSNESS ( 9 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
AKATHISIA ( 8 FDA reports)
BIPOLAR DISORDER ( 8 FDA reports)
BLOOD GLUCOSE DECREASED ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
CYSTITIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
ENTERITIS INFECTIOUS ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
GASTRIC CANCER ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 8 FDA reports)
IMPULSIVE BEHAVIOUR ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LONG QT SYNDROME ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 8 FDA reports)
NEOPLASM PROGRESSION ( 8 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 8 FDA reports)
SHUNT MALFUNCTION ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
ACTIVATION SYNDROME ( 7 FDA reports)
ALCOHOL POISONING ( 7 FDA reports)
ANGER ( 7 FDA reports)
BLOOD CHLORIDE DECREASED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
CHILLS ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERAMMONAEMIA ( 7 FDA reports)
LACERATION ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
MULTIPLE SCLEROSIS ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
NOCTURIA ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PROTEINURIA ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RETINAL HAEMORRHAGE ( 7 FDA reports)
RHEUMATOID ARTHRITIS ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
TUMOUR LYSIS SYNDROME ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
UTERINE LEIOMYOMA ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
FACIAL SPASM ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GOITRE ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPERCREATININAEMIA ( 6 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 6 FDA reports)
JOINT ANKYLOSIS ( 6 FDA reports)
LARYNGEAL OEDEMA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
PAIN ( 6 FDA reports)
PNEUMOMEDIASTINUM ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
QUADRIPLEGIA ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ANURIA ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
CANCER PAIN ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DYSKINESIA NEONATAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GASTRIC ULCER PERFORATION ( 5 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 5 FDA reports)
GENITAL HAEMORRHAGE ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MONONEUROPATHY MULTIPLEX ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
MUSCLE CONTRACTURE ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
NEONATAL RESPIRATORY ARREST ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
ORAL INTAKE REDUCED ( 5 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PARAESTHESIA ORAL ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
THIRST ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
VENOUS THROMBOSIS LIMB ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
WOUND ( 5 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABORTION MISSED ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
APATHY ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BRAIN CONTUSION ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHORIORETINAL ATROPHY ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EAR MALFORMATION ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING GUILTY ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PORIOMANIA ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN SWELLING ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
SPUTUM RETENTION ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SWEAT GLAND DISORDER ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLAST CELLS PRESENT ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CRANIOTABES ( 3 FDA reports)
CYST ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
ERYTHEMA ANNULARE ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FAT ATROPHY ( 3 FDA reports)
FEAR ( 3 FDA reports)
FINGER HYPOPLASIA ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
ICHTHYOSIS ACQUIRED ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
JEJUNAL PERFORATION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSEUDOALDOSTERONISM ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
RADIATION PNEUMONITIS ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SELF MUTILATION ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STRESS ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TENSION ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VENA CAVA FILTER INSERTION ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BIPOLAR II DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
C-REACTIVE PROTEIN ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL LESION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISUSE SYNDROME ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEPAPLASTIN ABNORMAL ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERURICOSURIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INABILITY TO CRAWL ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MECHANICAL ILEUS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEUROBLASTOMA RECURRENT ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL REVASCULARISATION ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERAL CATHETERISATION ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTI-INSULIN ANTIBODY ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOSYNCRATIC ALCOHOL INTOXICATION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE INDURATION ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUS IN STOOL ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYLORUS DILATATION ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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