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

VOMITING ( 153 FDA reports)
DYSPNOEA ( 152 FDA reports)
COMPLETED SUICIDE ( 129 FDA reports)
MALAISE ( 129 FDA reports)
DIZZINESS ( 119 FDA reports)
DRUG INTERACTION ( 116 FDA reports)
ABDOMINAL PAIN ( 115 FDA reports)
DIARRHOEA ( 104 FDA reports)
FATIGUE ( 104 FDA reports)
NAUSEA ( 100 FDA reports)
PAIN ( 98 FDA reports)
OEDEMA PERIPHERAL ( 92 FDA reports)
HYPOTENSION ( 88 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 87 FDA reports)
HEADACHE ( 85 FDA reports)
OVERDOSE ( 84 FDA reports)
HAEMOGLOBIN DECREASED ( 83 FDA reports)
RENAL FAILURE ACUTE ( 83 FDA reports)
MYOCARDIAL INFARCTION ( 82 FDA reports)
RASH ( 79 FDA reports)
PNEUMONIA ( 75 FDA reports)
ASTHENIA ( 74 FDA reports)
CHEST PAIN ( 70 FDA reports)
ATRIAL FIBRILLATION ( 69 FDA reports)
PRURITUS ( 66 FDA reports)
CEREBROVASCULAR ACCIDENT ( 64 FDA reports)
NEUTROPENIA ( 63 FDA reports)
HAEMATEMESIS ( 62 FDA reports)
SOMNOLENCE ( 62 FDA reports)
DEPRESSION ( 61 FDA reports)
HYPERTENSION ( 61 FDA reports)
PYREXIA ( 61 FDA reports)
RENAL FAILURE ( 61 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 59 FDA reports)
ANAEMIA ( 58 FDA reports)
GAIT DISTURBANCE ( 58 FDA reports)
RHABDOMYOLYSIS ( 57 FDA reports)
MYALGIA ( 56 FDA reports)
DEATH ( 55 FDA reports)
DRUG INEFFECTIVE ( 54 FDA reports)
ARTHRALGIA ( 53 FDA reports)
ERYTHEMA ( 53 FDA reports)
CONSTIPATION ( 51 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 50 FDA reports)
DYSPHAGIA ( 49 FDA reports)
HALLUCINATION ( 49 FDA reports)
PAIN IN EXTREMITY ( 49 FDA reports)
CORONARY ARTERY DISEASE ( 48 FDA reports)
DEHYDRATION ( 48 FDA reports)
BACK PAIN ( 47 FDA reports)
FALL ( 47 FDA reports)
CONFUSIONAL STATE ( 46 FDA reports)
CARDIAC FAILURE ( 45 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 45 FDA reports)
HYPERSENSITIVITY ( 45 FDA reports)
MEMORY IMPAIRMENT ( 45 FDA reports)
JAUNDICE ( 44 FDA reports)
HEPATIC FAILURE ( 43 FDA reports)
LOSS OF CONSCIOUSNESS ( 42 FDA reports)
MEDICATION ERROR ( 42 FDA reports)
URINARY TRACT INFECTION ( 42 FDA reports)
DRUG ABUSE ( 41 FDA reports)
DRUG TOXICITY ( 41 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 41 FDA reports)
BLOOD CREATININE INCREASED ( 40 FDA reports)
TREMOR ( 40 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 39 FDA reports)
SEPSIS ( 39 FDA reports)
ABDOMINAL PAIN UPPER ( 38 FDA reports)
CARDIAC ARREST ( 38 FDA reports)
LETHARGY ( 38 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 37 FDA reports)
PARAESTHESIA ( 37 FDA reports)
ABNORMAL BEHAVIOUR ( 36 FDA reports)
CHROMATURIA ( 36 FDA reports)
HEPATIC NECROSIS ( 36 FDA reports)
WEIGHT DECREASED ( 36 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 35 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 35 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 35 FDA reports)
AGITATION ( 34 FDA reports)
ANAPHYLACTIC REACTION ( 34 FDA reports)
EPISTAXIS ( 34 FDA reports)
HYPERHIDROSIS ( 34 FDA reports)
NEUTROPENIC SEPSIS ( 34 FDA reports)
POISONING ( 34 FDA reports)
BLISTER ( 33 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 33 FDA reports)
DUODENAL ULCER ( 33 FDA reports)
URINARY INCONTINENCE ( 33 FDA reports)
ANXIETY ( 32 FDA reports)
DECREASED APPETITE ( 32 FDA reports)
HAEMATOCHEZIA ( 32 FDA reports)
INFECTION ( 32 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 32 FDA reports)
MYOSITIS ( 31 FDA reports)
PULMONARY EMBOLISM ( 31 FDA reports)
PULMONARY FIBROSIS ( 31 FDA reports)
RASH GENERALISED ( 31 FDA reports)
SYNCOPE ( 31 FDA reports)
AMNESIA ( 30 FDA reports)
CEREBRAL INFARCTION ( 30 FDA reports)
CONDITION AGGRAVATED ( 30 FDA reports)
PSORIASIS ( 30 FDA reports)
ABDOMINAL DISTENSION ( 29 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 29 FDA reports)
HYPERKALAEMIA ( 29 FDA reports)
MULTIPLE DRUG OVERDOSE ( 29 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 28 FDA reports)
CELLULITIS ( 28 FDA reports)
MULTI-ORGAN FAILURE ( 28 FDA reports)
PALPITATIONS ( 28 FDA reports)
PANCREATITIS ( 28 FDA reports)
ACUTE HEPATIC FAILURE ( 27 FDA reports)
ANGINA PECTORIS ( 27 FDA reports)
CARDIO-RESPIRATORY ARREST ( 27 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 27 FDA reports)
CIRCULATORY COLLAPSE ( 27 FDA reports)
DEEP VEIN THROMBOSIS ( 27 FDA reports)
ECZEMA ( 27 FDA reports)
JOINT SWELLING ( 27 FDA reports)
RENAL IMPAIRMENT ( 27 FDA reports)
RESTLESSNESS ( 27 FDA reports)
STEVENS-JOHNSON SYNDROME ( 27 FDA reports)
TACHYCARDIA ( 27 FDA reports)
THROMBOCYTOPENIA ( 27 FDA reports)
CARDIAC DISORDER ( 26 FDA reports)
FLUID OVERLOAD ( 26 FDA reports)
INTERSTITIAL LUNG DISEASE ( 26 FDA reports)
INTRA-UTERINE DEATH ( 26 FDA reports)
MACROCYTOSIS ( 26 FDA reports)
METABOLIC ACIDOSIS ( 26 FDA reports)
MOUTH ULCERATION ( 26 FDA reports)
MYOCARDIAL ISCHAEMIA ( 26 FDA reports)
VISION BLURRED ( 26 FDA reports)
WEIGHT INCREASED ( 26 FDA reports)
BRONCHOPNEUMONIA ( 25 FDA reports)
DRUG ADMINISTRATION ERROR ( 25 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
DRY MOUTH ( 24 FDA reports)
ENTERITIS ( 24 FDA reports)
HYPOXIA ( 24 FDA reports)
MELAENA ( 24 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 24 FDA reports)
SWOLLEN TONGUE ( 24 FDA reports)
ACCIDENTAL OVERDOSE ( 23 FDA reports)
COLITIS ISCHAEMIC ( 23 FDA reports)
ERECTILE DYSFUNCTION ( 23 FDA reports)
HALLUCINATION, VISUAL ( 23 FDA reports)
HYPOKINESIA ( 23 FDA reports)
OSTEONECROSIS ( 23 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 23 FDA reports)
PULMONARY OEDEMA ( 23 FDA reports)
SCAB ( 23 FDA reports)
TINNITUS ( 23 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 23 FDA reports)
ABORTION SPONTANEOUS ( 22 FDA reports)
AGGRESSION ( 22 FDA reports)
BLOOD UREA INCREASED ( 22 FDA reports)
CONVULSION ( 22 FDA reports)
DEAFNESS NEUROSENSORY ( 22 FDA reports)
FEELING ABNORMAL ( 22 FDA reports)
GASTRIC ULCER ( 22 FDA reports)
MOBILITY DECREASED ( 22 FDA reports)
RASH MACULO-PAPULAR ( 22 FDA reports)
RESPIRATORY FAILURE ( 22 FDA reports)
ACIDOSIS ( 21 FDA reports)
ANGIOEDEMA ( 21 FDA reports)
ASCITES ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
BRADYCARDIA ( 21 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 21 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
INSOMNIA ( 21 FDA reports)
PALLOR ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
URTICARIA ( 21 FDA reports)
ABDOMINAL TENDERNESS ( 20 FDA reports)
BLOOD BILIRUBIN INCREASED ( 20 FDA reports)
CHILLS ( 20 FDA reports)
CONTUSION ( 20 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 20 FDA reports)
LEUKOPENIA ( 20 FDA reports)
PLATELET COUNT DECREASED ( 20 FDA reports)
RESPIRATORY ARREST ( 20 FDA reports)
RHEUMATOID ARTHRITIS ( 20 FDA reports)
SUICIDE ATTEMPT ( 20 FDA reports)
BLOOD PRESSURE INCREASED ( 19 FDA reports)
DRY SKIN ( 19 FDA reports)
HYPERLIPIDAEMIA ( 19 FDA reports)
HYPONATRAEMIA ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
LIP SWELLING ( 19 FDA reports)
PURPURA ( 19 FDA reports)
RASH PRURITIC ( 19 FDA reports)
SWELLING FACE ( 19 FDA reports)
ALOPECIA ( 18 FDA reports)
APHTHOUS STOMATITIS ( 18 FDA reports)
DYSPEPSIA ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
IRRITABILITY ( 18 FDA reports)
NEUTROPHIL COUNT DECREASED ( 18 FDA reports)
PANCREATITIS ACUTE ( 18 FDA reports)
PETECHIAE ( 18 FDA reports)
SKIN EXFOLIATION ( 18 FDA reports)
SUICIDAL IDEATION ( 18 FDA reports)
SWELLING ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
YELLOW SKIN ( 18 FDA reports)
BLOOD SODIUM DECREASED ( 17 FDA reports)
DRUG DEPENDENCE ( 17 FDA reports)
EXFOLIATIVE RASH ( 17 FDA reports)
MUSCLE SPASMS ( 17 FDA reports)
NECK PAIN ( 17 FDA reports)
UNRESPONSIVE TO STIMULI ( 17 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 16 FDA reports)
COUGH ( 16 FDA reports)
CYST ( 16 FDA reports)
DIVERTICULITIS ( 16 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 16 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 16 FDA reports)
HYPERSOMNIA ( 16 FDA reports)
LABILE BLOOD PRESSURE ( 16 FDA reports)
MIGRAINE ( 16 FDA reports)
OEDEMA ( 16 FDA reports)
SLEEP DISORDER ( 16 FDA reports)
THIRST ( 16 FDA reports)
ARTHRITIS ( 15 FDA reports)
CEREBRAL HAEMORRHAGE ( 15 FDA reports)
COMA ( 15 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 15 FDA reports)
DEPENDENCE ( 15 FDA reports)
FAECES DISCOLOURED ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
HYPOGLYCAEMIA ( 15 FDA reports)
INJURY ( 15 FDA reports)
OCULAR HYPERAEMIA ( 15 FDA reports)
PANCYTOPENIA ( 15 FDA reports)
ABDOMINAL RIGIDITY ( 14 FDA reports)
APHASIA ( 14 FDA reports)
DYSARTHRIA ( 14 FDA reports)
EOSINOPHILIA ( 14 FDA reports)
EPILEPSY ( 14 FDA reports)
GASTROINTESTINAL DISORDER ( 14 FDA reports)
HAEMATURIA ( 14 FDA reports)
HEART RATE DECREASED ( 14 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 14 FDA reports)
HIATUS HERNIA ( 14 FDA reports)
HYPOPHAGIA ( 14 FDA reports)
INADEQUATE ANALGESIA ( 14 FDA reports)
INTENTIONAL OVERDOSE ( 14 FDA reports)
MUSCULAR WEAKNESS ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
STAPHYLOCOCCAL INFECTION ( 14 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 14 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 14 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
ACUTE CORONARY SYNDROME ( 13 FDA reports)
APNOEA ( 13 FDA reports)
BALANCE DISORDER ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
LIVER INJURY ( 13 FDA reports)
LOSS OF LIBIDO ( 13 FDA reports)
MOUTH CYST ( 13 FDA reports)
NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
OSTEOARTHRITIS ( 13 FDA reports)
OSTEOMYELITIS ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
SINUSITIS ( 13 FDA reports)
SKIN DISORDER ( 13 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 12 FDA reports)
COAGULOPATHY ( 12 FDA reports)
CYTOLYTIC HEPATITIS ( 12 FDA reports)
DIABETES MELLITUS ( 12 FDA reports)
FEELING HOT ( 12 FDA reports)
HEART RATE INCREASED ( 12 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 12 FDA reports)
MASS ( 12 FDA reports)
SLEEP TALKING ( 12 FDA reports)
SOMNAMBULISM ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ABASIA ( 11 FDA reports)
ANGER ( 11 FDA reports)
DIABETIC RETINOPATHY ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
DRUG ERUPTION ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 11 FDA reports)
FEELING COLD ( 11 FDA reports)
HEPATITIS ( 11 FDA reports)
INTESTINAL ISCHAEMIA ( 11 FDA reports)
LEFT VENTRICULAR FAILURE ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MICTURITION DISORDER ( 11 FDA reports)
MIOSIS ( 11 FDA reports)
PLATELET COUNT INCREASED ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
TRANSPLANT FAILURE ( 11 FDA reports)
VENTRICULAR DYSFUNCTION ( 11 FDA reports)
WHEEZING ( 11 FDA reports)
AGEUSIA ( 10 FDA reports)
ASTHMA ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 10 FDA reports)
DYSLIPIDAEMIA ( 10 FDA reports)
DYSSTASIA ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
GOUT ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
HEPATIC ENCEPHALOPATHY ( 10 FDA reports)
INTENTIONAL MISUSE ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
LARGE INTESTINE PERFORATION ( 10 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
LYMPHADENOPATHY ( 10 FDA reports)
PREGNANCY ( 10 FDA reports)
SKIN DISCOLOURATION ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
ARTHROPATHY ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
DEMYELINATION ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HIP DYSPLASIA ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
INCORRECT DOSE ADMINISTERED ( 9 FDA reports)
INFLUENZA LIKE ILLNESS ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LYMPHADENITIS ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
OESOPHAGITIS ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
PSYCHOTIC DISORDER ( 9 FDA reports)
RESPIRATORY DEPRESSION ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SKIN REACTION ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
TARDIVE DYSKINESIA ( 9 FDA reports)
TENDERNESS ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
AORTIC ANEURYSM ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BLOOD LACTIC ACID INCREASED ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
DEPRESSED MOOD ( 8 FDA reports)
DIABETIC MICROANGIOPATHY ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
DRUG DISPENSING ERROR ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 8 FDA reports)
ERYTHRODERMIC PSORIASIS ( 8 FDA reports)
FAECES PALE ( 8 FDA reports)
FIBROSIS ( 8 FDA reports)
HEART RATE IRREGULAR ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
KNEE ARTHROPLASTY ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
MACULAR DEGENERATION ( 8 FDA reports)
MEAN CELL VOLUME INCREASED ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
NEPHROLITHIASIS ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
SOPOR ( 8 FDA reports)
URINE AMPHETAMINE POSITIVE ( 8 FDA reports)
URINE COLOUR ABNORMAL ( 8 FDA reports)
WITHDRAWAL SYNDROME ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
APLASIA ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BRADYPNOEA ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
BREAST CANCER IN SITU ( 7 FDA reports)
CANDIDIASIS ( 7 FDA reports)
CARDIAC MURMUR ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 7 FDA reports)
COMA SCALE ABNORMAL ( 7 FDA reports)
DEPRESSION SUICIDAL ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
ISCHAEMIC STROKE ( 7 FDA reports)
MITRAL VALVE PROLAPSE ( 7 FDA reports)
MOVEMENT DISORDER ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
OBESITY ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PHARYNGEAL ERYTHEMA ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
SEDATION ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
SYSTOLIC DYSFUNCTION ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
APATHY ( 6 FDA reports)
ATHEROSCLEROSIS ( 6 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
FOETAL DEATH ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HYPOCALCAEMIA ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LUMBAR RADICULOPATHY ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
MYOGLOBIN URINE PRESENT ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 6 FDA reports)
PAPILLARY THYROID CANCER ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PENILE SWELLING ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SCROTAL SWELLING ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
STRESS ( 6 FDA reports)
TENSION ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
TYPE I HYPERSENSITIVITY ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VENA CAVA THROMBOSIS ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABDOMINAL HERNIA ( 5 FDA reports)
ABNORMAL DREAMS ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
BASOPHIL COUNT DECREASED ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BLUNTED AFFECT ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CAROTID ARTERY STENOSIS ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CRYING ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DIABETIC EYE DISEASE ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
EMOTIONAL POVERTY ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
LOCALISED OSTEOARTHRITIS ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MANIA ( 5 FDA reports)
MENTAL IMPAIRMENT ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MONOCYTE COUNT DECREASED ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MYOGLOBIN URINE ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PSORIATIC ARTHROPATHY ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
SEROTONIN SYNDROME ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
ULCER ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ACQUIRED HAEMOPHILIA ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BONE DISORDER ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CRYSTALLURIA ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENCEPHALITIS TOXIC ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FEAR ( 4 FDA reports)
FORCEPS DELIVERY ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GLOSSITIS ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LIVIDITY ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MENOMETRORRHAGIA ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEOVASCULARISATION ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NODULE ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PELVIC DEFORMITY ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
POLYCYTHAEMIA ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROSTATISM ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SKIN MASS ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SNORING ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIORENAL SYNDROME ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DACTYLITIS ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DEVICE EXPULSION ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
ERB'S PALSY ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER NECROSIS ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GENITAL INFECTION FEMALE ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORTHOPEDIC PROCEDURE ( 3 FDA reports)
OSMOLAR GAP ABNORMAL ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SHOULDER DYSTOCIA ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SPLINTER HAEMORRHAGES ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADHESION ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANDROGENETIC ALOPECIA ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASSISTED DELIVERY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBROVASCULAR SPASM ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELAYED DELIVERY ( 2 FDA reports)
DERMAL SINUS ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INJECTION SITE EXFOLIATION ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
MALIGNANT NEOPLASM OF CORNEA ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MEDICAL OBSERVATION ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL SINUS CANCER ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NEEDLE TRACK MARKS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA STAGE II ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARKINSONIAN CRISIS ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE EJACULATION ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINAL SCAR ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SEXUAL ABUSE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL DECOMPRESSION ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE PRURITUS ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANASTOMOTIC FISTULA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BASE EXCESS ABNORMAL ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOROID PLEXUS PAPILLOMA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CYP2C19 POLYMORPHISM ( 1 FDA reports)
CYP2D6 POLYMORPHISM ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIARRHOEA NEONATAL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYEBALL AVULSION ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUPUS HEPATITIS ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC ATHEROSCLEROSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POST COITAL BLEEDING ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTPARTUM VENOUS THROMBOSIS ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERMOMETRY ABNORMAL ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

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