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

PYREXIA ( 61 FDA reports)
ANAEMIA ( 45 FDA reports)
DYSPNOEA ( 45 FDA reports)
NAUSEA ( 43 FDA reports)
PRURITUS ( 42 FDA reports)
VOMITING ( 41 FDA reports)
FATIGUE ( 39 FDA reports)
DIARRHOEA ( 38 FDA reports)
HEADACHE ( 38 FDA reports)
RENAL FAILURE ACUTE ( 36 FDA reports)
FALL ( 35 FDA reports)
CONDITION AGGRAVATED ( 34 FDA reports)
DRUG INTERACTION ( 31 FDA reports)
RASH ( 31 FDA reports)
ASTHENIA ( 29 FDA reports)
CONFUSIONAL STATE ( 29 FDA reports)
ERYTHEMA ( 29 FDA reports)
CYTOLYTIC HEPATITIS ( 28 FDA reports)
ABDOMINAL PAIN ( 27 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 26 FDA reports)
ASTHMA ( 25 FDA reports)
LUNG DISORDER ( 25 FDA reports)
ANGIOEDEMA ( 24 FDA reports)
ARTHRALGIA ( 24 FDA reports)
MALAISE ( 24 FDA reports)
INFUSION RELATED REACTION ( 23 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 22 FDA reports)
HYPONATRAEMIA ( 22 FDA reports)
HYPOTENSION ( 22 FDA reports)
COUGH ( 21 FDA reports)
RASH MACULO-PAPULAR ( 21 FDA reports)
RENAL FAILURE ( 21 FDA reports)
OEDEMA PERIPHERAL ( 20 FDA reports)
PARAESTHESIA ( 20 FDA reports)
WEIGHT DECREASED ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
HYPERSENSITIVITY ( 19 FDA reports)
TOXIC SKIN ERUPTION ( 19 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 18 FDA reports)
ECZEMA ( 18 FDA reports)
SOMNOLENCE ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 17 FDA reports)
URTICARIA ( 17 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
CYANOSIS ( 16 FDA reports)
FACE OEDEMA ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 16 FDA reports)
THROMBOCYTOPENIA ( 16 FDA reports)
DEPRESSION ( 15 FDA reports)
GAIT DISTURBANCE ( 15 FDA reports)
HYPERKALAEMIA ( 15 FDA reports)
PAIN ( 15 FDA reports)
RESPIRATORY DISORDER ( 15 FDA reports)
SEPTIC SHOCK ( 15 FDA reports)
SUICIDE ATTEMPT ( 15 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
DEHYDRATION ( 14 FDA reports)
EOSINOPHILIA ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
PURPURA ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
CHILLS ( 13 FDA reports)
HYPERTENSION ( 13 FDA reports)
INFLUENZA LIKE ILLNESS ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
THROMBOSIS ( 13 FDA reports)
BRADYCARDIA ( 12 FDA reports)
BRONCHITIS ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
BACK PAIN ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
GASTRIC ULCER ( 11 FDA reports)
HAEMATOMA ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
MYALGIA ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
ASCITES ( 10 FDA reports)
ASTHMATIC CRISIS ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
HYPOGLYCAEMIA ( 10 FDA reports)
INFLAMMATION ( 10 FDA reports)
LUNG INFECTION ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PRODUCT QUALITY ISSUE ( 10 FDA reports)
VISUAL ACUITY REDUCED ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
AGGRESSION ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
PRURIGO ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
COARCTATION OF THE AORTA ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
GASTROINTESTINAL MALFORMATION ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
HYPOVOLAEMIA ( 8 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
OESOPHAGEAL ATRESIA ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
SHOCK ( 8 FDA reports)
TREMOR ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
CELL DEATH ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
DERMATITIS EXFOLIATIVE ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
GAMMOPATHY ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
MYOPATHY ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RAYNAUD'S PHENOMENON ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
ANURIA ( 6 FDA reports)
APHASIA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
CONCUSSION ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPERKINESIA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
OCULAR HYPERAEMIA ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
AGITATION ( 5 FDA reports)
APALLIC SYNDROME ( 5 FDA reports)
APNOEA ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BIOPSY SKIN ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BURNS THIRD DEGREE ( 5 FDA reports)
CARDIAC FIBRILLATION ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CEREBROVASCULAR DISORDER ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
COMA ( 5 FDA reports)
DEATH ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
NASAL CONGESTION ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
OXYGEN SATURATION ABNORMAL ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PREMATURE MENOPAUSE ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
TRACHEAL INJURY ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
APHONIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
DECREASED VIBRATORY SENSE ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ERYTHEMA INFECTIOSUM ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TOOTH DISCOLOURATION ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL BRUIT ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACCIDENT AT HOME ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FIBRINOLYSIS ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHILLBLAINS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CRANIAL NERVE INFECTION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOLLICULAR MUCINOSIS ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCAL REACTION ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MENOPAUSAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOCUTANEOUS ULCERATION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROBLASTOMA ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OCULAR TOXICITY ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PO2 ABNORMAL ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
TETANY ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITAMIN K ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WITHDRAWAL ARRHYTHMIA ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BARTHOLIN'S ABSCESS ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN ANTI-MOUSE ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL STRICTURE ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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