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

PYREXIA ( 82 FDA reports)
RASH ( 76 FDA reports)
RENAL FAILURE ACUTE ( 72 FDA reports)
DIARRHOEA ( 64 FDA reports)
PRURITUS ( 55 FDA reports)
VOMITING ( 46 FDA reports)
ERYTHEMA ( 45 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 44 FDA reports)
DRUG INTERACTION ( 42 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 39 FDA reports)
CHOLESTASIS ( 35 FDA reports)
MALAISE ( 35 FDA reports)
ABDOMINAL PAIN ( 34 FDA reports)
HEADACHE ( 32 FDA reports)
JAUNDICE ( 32 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
NAUSEA ( 30 FDA reports)
CONDITION AGGRAVATED ( 29 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 29 FDA reports)
DYSPNOEA ( 29 FDA reports)
EOSINOPHILIA ( 29 FDA reports)
ANGIOEDEMA ( 28 FDA reports)
ANOREXIA ( 27 FDA reports)
DRUG ERUPTION ( 27 FDA reports)
THROMBOCYTOPENIA ( 27 FDA reports)
DRUG HYPERSENSITIVITY ( 26 FDA reports)
OEDEMA PERIPHERAL ( 26 FDA reports)
LIVER DISORDER ( 25 FDA reports)
RENAL FAILURE ( 25 FDA reports)
STEVENS-JOHNSON SYNDROME ( 25 FDA reports)
TOXIC SKIN ERUPTION ( 25 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 24 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 24 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 24 FDA reports)
NEUTROPENIA ( 24 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
INFLAMMATION ( 23 FDA reports)
RASH MACULO-PAPULAR ( 23 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 22 FDA reports)
HEPATIC STEATOSIS ( 22 FDA reports)
PAIN ( 22 FDA reports)
URTICARIA ( 22 FDA reports)
BLOOD BILIRUBIN INCREASED ( 21 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
HEPATOMEGALY ( 21 FDA reports)
MEDICATION ERROR ( 21 FDA reports)
AGRANULOCYTOSIS ( 20 FDA reports)
CONFUSIONAL STATE ( 20 FDA reports)
SKIN EXFOLIATION ( 20 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 19 FDA reports)
DEHYDRATION ( 19 FDA reports)
DERMATITIS EXFOLIATIVE ( 19 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 19 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 19 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 18 FDA reports)
BRADYCARDIA ( 18 FDA reports)
CAESAREAN SECTION ( 18 FDA reports)
CONJUNCTIVITIS ( 18 FDA reports)
HAEMATOMA ( 18 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
SKIN TEST POSITIVE ( 18 FDA reports)
DEATH ( 17 FDA reports)
DEPRESSION ( 17 FDA reports)
ERYTHEMA MULTIFORME ( 17 FDA reports)
FACE OEDEMA ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
LYMPHADENOPATHY ( 17 FDA reports)
PANCYTOPENIA ( 17 FDA reports)
PROTEINURIA ( 17 FDA reports)
BRONCHITIS ( 16 FDA reports)
CONVULSION ( 16 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 16 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 16 FDA reports)
LEUKOCYTOSIS ( 16 FDA reports)
OVERDOSE ( 16 FDA reports)
SUICIDE ATTEMPT ( 16 FDA reports)
WRONG DRUG ADMINISTERED ( 16 FDA reports)
ANAPHYLACTIC SHOCK ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
DYSPHAGIA ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
URINARY TRACT INFECTION ( 15 FDA reports)
BLISTER ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 14 FDA reports)
FALL ( 14 FDA reports)
GENERALISED ERYTHEMA ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPERSENSITIVITY ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
ANXIETY ( 13 FDA reports)
BRONCHOSPASM ( 13 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 13 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
LARYNGEAL OEDEMA ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 13 FDA reports)
PURPURA ( 13 FDA reports)
ASCITES ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
ILL-DEFINED DISORDER ( 12 FDA reports)
PANCREATITIS ACUTE ( 12 FDA reports)
PREMATURE BABY ( 12 FDA reports)
RASH ERYTHEMATOUS ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
RASH MACULAR ( 12 FDA reports)
RASH PRURITIC ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
DIZZINESS ( 11 FDA reports)
HYPERTHERMIA ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
SKIN LESION ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
AGITATION ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
HEPATOTOXICITY ( 10 FDA reports)
OFF LABEL USE ( 10 FDA reports)
RASH PUSTULAR ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
ACUTE TONSILLITIS ( 9 FDA reports)
ASTHMA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
FEELING HOT ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
INFECTION ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MELAENA ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
RALES ( 9 FDA reports)
SINUSITIS ( 9 FDA reports)
TREMOR ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
RHINITIS ( 8 FDA reports)
STILLBIRTH ( 8 FDA reports)
UNRESPONSIVE TO STIMULI ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHROMATURIA ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
HAEMOLYSIS ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
NEPHRITIS INTERSTITIAL ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
COUGH ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DERMATITIS ALLERGIC ( 6 FDA reports)
DIALYSIS ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PRURIGO ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
REFLUX OESOPHAGITIS ( 6 FDA reports)
SCAR ( 6 FDA reports)
SERUM SICKNESS ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
STREPTOCOCCAL INFECTION ( 6 FDA reports)
X-RAY ABNORMAL ( 6 FDA reports)
ABORTION ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
ANTI FACTOR V ANTIBODY POSITIVE ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
COMA ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
EPIDERMOLYSIS ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ANASTOMOTIC STENOSIS ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANURIA ( 4 FDA reports)
APHASIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSTHYMIC DISORDER ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
ERYTHROMELALGIA ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
KAWASAKI'S DISEASE ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
ULCER ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINOMA ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACETONAEMIC VOMITING ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
AMIMIA ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAL ATRESIA ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BILIRUBIN CONJUGATED ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORNEAL REFLEX DECREASED ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
ILEUS ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PSYCHOTIC BEHAVIOUR ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THYMUS DISORDER ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URETHRAL FISTULA ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLEEDING ANOVULATORY ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE MARROW NECROSIS ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYST ( 2 FDA reports)
CYTOKINE RELEASE SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KOUNIS SYNDROME ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MANIA ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MEDIASTINAL ABSCESS ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHORTENED CERVIX ( 2 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STRESS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TERATOGENICITY ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AURA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CEREBRAL GAS EMBOLISM ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX NEOPLASM ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION MALE ( 1 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 1 FDA reports)
CONGENITAL SKIN DISORDER ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS AMYLOIDOSIS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL MALNUTRITION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGE NEONATAL ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPHTHALMIA NEONATORUM ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAMETRIC ABSCESS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARAPHARYNGEAL ABSCESS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL NECROSIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
REYE'S SYNDROME ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TETANY ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS BACTERIAL ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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