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

DERMATITIS ACNEIFORM ( 166 FDA reports)
INFUSION RELATED REACTION ( 159 FDA reports)
VOMITING ( 120 FDA reports)
PRURITUS ( 107 FDA reports)
CHEST PAIN ( 106 FDA reports)
RASH ( 105 FDA reports)
NAUSEA ( 104 FDA reports)
DIARRHOEA ( 97 FDA reports)
DYSPNOEA ( 97 FDA reports)
COLORECTAL CANCER ( 93 FDA reports)
STOMATITIS ( 93 FDA reports)
HYPOXIA ( 85 FDA reports)
HEADACHE ( 84 FDA reports)
PYREXIA ( 81 FDA reports)
BACK PAIN ( 75 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 64 FDA reports)
ALOPECIA ( 63 FDA reports)
APPENDICITIS ( 63 FDA reports)
CHILLS ( 63 FDA reports)
DECREASED APPETITE ( 63 FDA reports)
GASTROENTERITIS ( 63 FDA reports)
INFLAMMATION ( 61 FDA reports)
DRY SKIN ( 58 FDA reports)
INTERSTITIAL LUNG DISEASE ( 57 FDA reports)
PARONYCHIA ( 57 FDA reports)
ANAEMIA ( 54 FDA reports)
PAIN ( 51 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 47 FDA reports)
HYPERHIDROSIS ( 47 FDA reports)
CROHN'S DISEASE ( 46 FDA reports)
HYPOMAGNESAEMIA ( 46 FDA reports)
MALAISE ( 46 FDA reports)
FATIGUE ( 45 FDA reports)
PALPITATIONS ( 44 FDA reports)
OSTEOPOROSIS ( 43 FDA reports)
PLATELET COUNT DECREASED ( 43 FDA reports)
NEUTROPHIL COUNT DECREASED ( 42 FDA reports)
PNEUMONIA ( 42 FDA reports)
THYROID CANCER ( 42 FDA reports)
HYPOTENSION ( 41 FDA reports)
DEPRESSION ( 40 FDA reports)
ARTHRALGIA ( 38 FDA reports)
DIZZINESS ( 38 FDA reports)
ANXIETY ( 37 FDA reports)
INSOMNIA ( 37 FDA reports)
URTICARIA ( 37 FDA reports)
BREAST CANCER ( 36 FDA reports)
DRUG INEFFECTIVE ( 36 FDA reports)
RENAL FAILURE ACUTE ( 36 FDA reports)
SPINAL COMPRESSION FRACTURE ( 36 FDA reports)
ABDOMINAL PAIN ( 35 FDA reports)
HERPES ZOSTER ( 33 FDA reports)
HYPOAESTHESIA ( 33 FDA reports)
NEUROPATHY PERIPHERAL ( 33 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 32 FDA reports)
COUGH ( 31 FDA reports)
HAEMOGLOBIN DECREASED ( 31 FDA reports)
OEDEMA PERIPHERAL ( 31 FDA reports)
BEHCET'S SYNDROME ( 30 FDA reports)
COMPLETED SUICIDE ( 30 FDA reports)
HYPOCALCAEMIA ( 30 FDA reports)
DEHYDRATION ( 29 FDA reports)
ERYTHEMA ( 29 FDA reports)
TACHYCARDIA ( 29 FDA reports)
DEATH ( 28 FDA reports)
FLUSHING ( 28 FDA reports)
BRONCHITIS ( 27 FDA reports)
FEBRILE NEUTROPENIA ( 27 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 27 FDA reports)
OSTEONECROSIS OF JAW ( 27 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 27 FDA reports)
ANGINA PECTORIS ( 25 FDA reports)
DERMATITIS ( 25 FDA reports)
HYPOKALAEMIA ( 25 FDA reports)
MYALGIA ( 25 FDA reports)
ANGIOEDEMA ( 24 FDA reports)
HAEMATOCRIT DECREASED ( 24 FDA reports)
NEOPLASM MALIGNANT ( 24 FDA reports)
URINARY TRACT INFECTION ( 24 FDA reports)
OSTEOMYELITIS ( 23 FDA reports)
WEIGHT DECREASED ( 23 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 22 FDA reports)
GLAUCOMA ( 22 FDA reports)
HYPERSENSITIVITY ( 22 FDA reports)
HYPERTENSION ( 22 FDA reports)
MUSCULAR WEAKNESS ( 22 FDA reports)
BLOOD GLUCOSE INCREASED ( 21 FDA reports)
ABDOMINAL PAIN UPPER ( 20 FDA reports)
ASTHENIA ( 20 FDA reports)
BLOOD PRESSURE DECREASED ( 20 FDA reports)
BONE DISORDER ( 20 FDA reports)
FEELING ABNORMAL ( 20 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 20 FDA reports)
DISCOMFORT ( 19 FDA reports)
INJECTION SITE ERYTHEMA ( 19 FDA reports)
MENTAL STATUS CHANGES ( 19 FDA reports)
RENAL FAILURE ( 19 FDA reports)
SINUSITIS ( 19 FDA reports)
BRAIN CANCER METASTATIC ( 18 FDA reports)
CONSTIPATION ( 18 FDA reports)
DYSARTHRIA ( 18 FDA reports)
GASTRIC MUCOSAL LESION ( 18 FDA reports)
LUNG CANCER METASTATIC ( 18 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
SWELLING ( 18 FDA reports)
TREMOR ( 18 FDA reports)
BLOOD PRESSURE INCREASED ( 17 FDA reports)
CELLULITIS ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
MYOCARDIAL INFARCTION ( 17 FDA reports)
POISONING ( 17 FDA reports)
RESPIRATORY ARREST ( 17 FDA reports)
SENSITIVITY OF TEETH ( 17 FDA reports)
SKIN EXFOLIATION ( 17 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 17 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
DYSPHAGIA ( 16 FDA reports)
JAUNDICE ( 16 FDA reports)
PNEUMONIA ASPIRATION ( 16 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 16 FDA reports)
SPINAL OSTEOARTHRITIS ( 16 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
ANAPHYLACTIC REACTION ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
DRY MOUTH ( 15 FDA reports)
DYSGEUSIA ( 15 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 15 FDA reports)
NEUTROPHIL COUNT INCREASED ( 15 FDA reports)
PULMONARY TUBERCULOSIS ( 15 FDA reports)
RENAL IMPAIRMENT ( 15 FDA reports)
SOMNOLENCE ( 15 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 14 FDA reports)
ALVEOLITIS ( 14 FDA reports)
ARTERIOSCLEROSIS ( 14 FDA reports)
BONE PAIN ( 14 FDA reports)
CEREBRAL INFARCTION ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
DECREASED INTEREST ( 14 FDA reports)
EOSINOPHIL COUNT DECREASED ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
GLOBULINS INCREASED ( 14 FDA reports)
LEUKODYSTROPHY ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
MONOCYTE COUNT DECREASED ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
PERIODONTAL DISEASE ( 14 FDA reports)
SKIN FISSURES ( 14 FDA reports)
TOOTH INFECTION ( 14 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 13 FDA reports)
BLOOD MAGNESIUM DECREASED ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 13 FDA reports)
FIBROMYALGIA ( 13 FDA reports)
GINGIVAL ULCERATION ( 13 FDA reports)
HAEMATOCHEZIA ( 13 FDA reports)
JOINT INJURY ( 13 FDA reports)
MOOD SWINGS ( 13 FDA reports)
MOUTH ULCERATION ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
NEUTROPENIA ( 13 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 13 FDA reports)
PREMATURE BABY ( 13 FDA reports)
RESTLESS LEGS SYNDROME ( 13 FDA reports)
SLEEP DISORDER ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
THYROID NEOPLASM ( 13 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 13 FDA reports)
AMNESIA ( 12 FDA reports)
ARRHYTHMIA ( 12 FDA reports)
BREAST CANCER METASTATIC ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
COSTOCHONDRITIS ( 12 FDA reports)
GINGIVITIS ( 12 FDA reports)
HYPOTHYROIDISM ( 12 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 12 FDA reports)
MONONEUROPATHY MULTIPLEX ( 12 FDA reports)
MORGANELLA INFECTION ( 12 FDA reports)
OESOPHAGITIS ( 12 FDA reports)
SHOCK ( 12 FDA reports)
SWELLING FACE ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
ACNE ( 11 FDA reports)
ATAXIA ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
DUODENAL ULCER ( 11 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 11 FDA reports)
FALL ( 11 FDA reports)
HEPATIC NEOPLASM ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
LYMPH NODE PALPABLE ( 11 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 11 FDA reports)
NECK MASS ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
PANCREATIC CYST ( 11 FDA reports)
SARCOIDOSIS ( 11 FDA reports)
SCOLIOSIS ( 11 FDA reports)
SKIN DISORDER ( 11 FDA reports)
ANAPHYLACTOID REACTION ( 10 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLADDER CANCER ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
DEAFNESS ( 10 FDA reports)
DYSPHONIA ( 10 FDA reports)
EAR PAIN ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
EMOTIONAL DISTRESS ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
INJECTION SITE PRURITUS ( 10 FDA reports)
INJECTION SITE SWELLING ( 10 FDA reports)
LARGE INTESTINE PERFORATION ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
NEPHROPATHY ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
SPINAL CORD COMPRESSION ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
ABDOMINAL ABSCESS ( 9 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
AGITATION ( 9 FDA reports)
ANAL FISTULA ( 9 FDA reports)
AORTIC STENOSIS ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
DISSEMINATED TUBERCULOSIS ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HYDRONEPHROSIS ( 9 FDA reports)
HYPERKERATOSIS ( 9 FDA reports)
ILEAL STENOSIS ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
INFLUENZA ( 9 FDA reports)
INFLUENZA LIKE ILLNESS ( 9 FDA reports)
LEFT ATRIAL DILATATION ( 9 FDA reports)
MASS ( 9 FDA reports)
METASTASES TO SPINE ( 9 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 9 FDA reports)
RASH ERYTHEMATOUS ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SKIN OEDEMA ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ABSCESS INTESTINAL ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
ASTHMA ( 8 FDA reports)
BLOOD CALCIUM DECREASED ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
COAGULOPATHY ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
CONGENITAL ECTODERMAL DYSPLASIA ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
ENTEROCUTANEOUS FISTULA ( 8 FDA reports)
HEARING IMPAIRED ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
INJURY ( 8 FDA reports)
INTESTINAL STENOSIS ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
MALIGNANT MELANOMA ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE ( 8 FDA reports)
NODULE ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
OTITIS MEDIA ACUTE ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
PRE-ECLAMPSIA ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
ACTINOMYCOSIS ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CATARACT ( 7 FDA reports)
CHROMATURIA ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
CYTOKINE RELEASE SYNDROME ( 7 FDA reports)
DENTAL FISTULA ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
EYE DISCHARGE ( 7 FDA reports)
FAT NECROSIS ( 7 FDA reports)
FOLATE DEFICIENCY ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
GLOSSITIS ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYPOGONADISM ( 7 FDA reports)
ILEUS ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LUNG NEOPLASM ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
LYMPHOEDEMA ( 7 FDA reports)
MELANOCYTIC NAEVUS ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUBACUTE ENDOCARDITIS ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TINEA PEDIS ( 7 FDA reports)
TOOTH EXTRACTION ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ABORTION SPONTANEOUS ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MUSCLE TWITCHING ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PAPULE ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PREMATURE DELIVERY ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 6 FDA reports)
SMALL INTESTINAL PERFORATION ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
VITAMIN B12 DEFICIENCY ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
ENTERITIS INFECTIOUS ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HAEMATOTOXICITY ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
INJECTION SITE INFLAMMATION ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
KLEBSIELLA INFECTION ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
MENOPAUSE ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CARDIAC HYPERTROPHY ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
HAEMOGLOBIN ABNORMAL ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
IMPLANT SITE NECROSIS ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RECTAL ABSCESS ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TOOTH FRACTURE ( 4 FDA reports)
VEIN PAIN ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANAESTHESIA DOLOROSA ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHONDROSARCOMA ( 3 FDA reports)
COMA ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DUODENAL OBSTRUCTION ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PERITONEAL ABSCESS ( 3 FDA reports)
PERITONEAL NEOPLASM ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL HYPERTROPHY ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BIOPSY BONE ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) RECURRENT ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HISTIOCYTOSIS ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPLANT SITE ERYTHEMA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOCARDIAL OEDEMA ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC DUCT STENOSIS ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCALCITONIN INCREASED ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
UROGRAM ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACHROMOTRICHIA ACQUIRED ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL CORTEX DYSPLASIA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 1 FDA reports)
ANGIOKERATOMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIAL DYSPLASIA ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPEDESIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS FUNGAL ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MID-LIFE CRISIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEISSERIA TEST POSITIVE ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMA CUTIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTERIOR INTEROSSEOUS SYNDROME ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STAG HORN CALCULUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYMUS HYPERTROPHY ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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