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

PYREXIA ( 231 FDA reports)
DIARRHOEA ( 229 FDA reports)
NAUSEA ( 167 FDA reports)
VOMITING ( 154 FDA reports)
ANAEMIA ( 144 FDA reports)
DRUG INTERACTION ( 124 FDA reports)
RASH ( 120 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 99 FDA reports)
HEADACHE ( 97 FDA reports)
ASTHENIA ( 89 FDA reports)
DYSPNOEA ( 89 FDA reports)
LIPODYSTROPHY ACQUIRED ( 88 FDA reports)
ABDOMINAL PAIN ( 87 FDA reports)
MALAISE ( 87 FDA reports)
COUGH ( 86 FDA reports)
FATIGUE ( 83 FDA reports)
RENAL FAILURE ACUTE ( 80 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 79 FDA reports)
WEIGHT DECREASED ( 76 FDA reports)
HYPERLIPIDAEMIA ( 75 FDA reports)
RENAL IMPAIRMENT ( 71 FDA reports)
DRUG INEFFECTIVE ( 70 FDA reports)
DRUG TOXICITY ( 69 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 68 FDA reports)
JAUNDICE ( 63 FDA reports)
HYPERTENSION ( 61 FDA reports)
HYPERSENSITIVITY ( 60 FDA reports)
MYALGIA ( 60 FDA reports)
MYOCARDIAL INFARCTION ( 60 FDA reports)
NEUTROPENIA ( 58 FDA reports)
RENAL FAILURE ( 56 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 55 FDA reports)
BLOOD BILIRUBIN INCREASED ( 51 FDA reports)
DRUG HYPERSENSITIVITY ( 50 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 50 FDA reports)
CACHEXIA ( 49 FDA reports)
COAGULATION TIME PROLONGED ( 48 FDA reports)
NEUROPATHY PERIPHERAL ( 48 FDA reports)
LYMPHADENOPATHY ( 47 FDA reports)
CONTUSION ( 46 FDA reports)
PREMATURE BABY ( 46 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 45 FDA reports)
PANCYTOPENIA ( 45 FDA reports)
RHABDOMYOLYSIS ( 44 FDA reports)
DIZZINESS ( 42 FDA reports)
LIVER DISORDER ( 42 FDA reports)
ORAL CANDIDIASIS ( 42 FDA reports)
PRURITUS ( 42 FDA reports)
SEPSIS ( 42 FDA reports)
HAEMOGLOBIN DECREASED ( 41 FDA reports)
DISEASE RECURRENCE ( 40 FDA reports)
DRUG RESISTANCE ( 40 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 40 FDA reports)
MYOPATHY ( 40 FDA reports)
LACTIC ACIDOSIS ( 39 FDA reports)
CHOLESTASIS ( 37 FDA reports)
HEPATIC FAILURE ( 37 FDA reports)
PHARYNGITIS ( 37 FDA reports)
THROMBOCYTOPENIA ( 37 FDA reports)
CHEST PAIN ( 36 FDA reports)
HYPOKALAEMIA ( 36 FDA reports)
OSTEONECROSIS ( 36 FDA reports)
PNEUMONIA ( 36 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 36 FDA reports)
DEATH ( 35 FDA reports)
OEDEMA PERIPHERAL ( 35 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 34 FDA reports)
BLOOD URIC ACID INCREASED ( 34 FDA reports)
BRADYCARDIA ( 34 FDA reports)
ABDOMINAL PAIN UPPER ( 33 FDA reports)
CARDIAC FAILURE ( 33 FDA reports)
DECREASED APPETITE ( 33 FDA reports)
HYPOTENSION ( 32 FDA reports)
PAIN ( 32 FDA reports)
HEPATIC ENCEPHALOPATHY ( 31 FDA reports)
NEPHROTIC SYNDROME ( 31 FDA reports)
PRODUCTIVE COUGH ( 31 FDA reports)
DEPRESSION ( 30 FDA reports)
HIV INFECTION ( 30 FDA reports)
PANCREATITIS ( 30 FDA reports)
PALLOR ( 29 FDA reports)
VIRAL LOAD INCREASED ( 29 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 28 FDA reports)
CHILLS ( 28 FDA reports)
CLEFT LIP AND PALATE ( 28 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 28 FDA reports)
HYPERLACTACIDAEMIA ( 28 FDA reports)
LIPOATROPHY ( 28 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 28 FDA reports)
PAIN IN EXTREMITY ( 28 FDA reports)
PROTEINURIA ( 28 FDA reports)
TACHYCARDIA ( 28 FDA reports)
ACUTE HEPATIC FAILURE ( 27 FDA reports)
AIDS ENCEPHALOPATHY ( 27 FDA reports)
ARTHRALGIA ( 27 FDA reports)
GASTROINTESTINAL DISORDER ( 27 FDA reports)
HEPATIC CIRRHOSIS ( 27 FDA reports)
HEPATOMEGALY ( 27 FDA reports)
LOSS OF CONSCIOUSNESS ( 27 FDA reports)
CONVULSION ( 26 FDA reports)
NERVOUS SYSTEM DISORDER ( 26 FDA reports)
SEPTIC SHOCK ( 26 FDA reports)
BLOOD CREATININE INCREASED ( 25 FDA reports)
CONDITION AGGRAVATED ( 25 FDA reports)
HEPATITIS ( 25 FDA reports)
HYPOAESTHESIA ( 25 FDA reports)
PLATELET COUNT DECREASED ( 25 FDA reports)
RASH GENERALISED ( 25 FDA reports)
SOMNOLENCE ( 25 FDA reports)
BLOOD AMYLASE INCREASED ( 24 FDA reports)
CAESAREAN SECTION ( 24 FDA reports)
CONFUSIONAL STATE ( 24 FDA reports)
PREGNANCY ( 24 FDA reports)
TRANSPLANT REJECTION ( 24 FDA reports)
DIABETES MELLITUS ( 23 FDA reports)
GUILLAIN-BARRE SYNDROME ( 23 FDA reports)
MITOCHONDRIAL TOXICITY ( 23 FDA reports)
NEPHROLITHIASIS ( 23 FDA reports)
PARAESTHESIA ( 23 FDA reports)
PORTAL HYPERTENSION ( 23 FDA reports)
TRANSAMINASES INCREASED ( 23 FDA reports)
ABORTION SPONTANEOUS ( 22 FDA reports)
BACK PAIN ( 22 FDA reports)
CARDIO-RESPIRATORY ARREST ( 22 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 22 FDA reports)
FANCONI SYNDROME ACQUIRED ( 22 FDA reports)
HEPATIC ENZYME INCREASED ( 22 FDA reports)
MELAENA ( 22 FDA reports)
MENTAL DISORDER ( 22 FDA reports)
ARRHYTHMIA ( 21 FDA reports)
ASCITES ( 21 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 21 FDA reports)
COGNITIVE DISORDER ( 21 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 21 FDA reports)
GASTRIC ULCER ( 21 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
GRAFT DYSFUNCTION ( 21 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 21 FDA reports)
INFLUENZA LIKE ILLNESS ( 21 FDA reports)
INSOMNIA ( 21 FDA reports)
PALPITATIONS ( 21 FDA reports)
PANCREATITIS ACUTE ( 21 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
DIPLOPIA ( 20 FDA reports)
METABOLIC ACIDOSIS ( 20 FDA reports)
NEPHRITIS INTERSTITIAL ( 20 FDA reports)
OCULAR ICTERUS ( 20 FDA reports)
OSTEOPOROSIS ( 20 FDA reports)
SPLENOMEGALY ( 20 FDA reports)
AGITATION ( 19 FDA reports)
HERPES ZOSTER ( 19 FDA reports)
RESPIRATORY FAILURE ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
BLOOD HIV RNA INCREASED ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
EYELID PTOSIS ( 18 FDA reports)
GAIT DISTURBANCE ( 18 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
TREATMENT NONCOMPLIANCE ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 17 FDA reports)
BLOOD LACTIC ACID INCREASED ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
KAPOSI'S SARCOMA ( 17 FDA reports)
LIVER TRANSPLANT ( 17 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 17 FDA reports)
STOMATITIS ( 17 FDA reports)
VISION BLURRED ( 17 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
BRONCHOPNEUMONIA ( 16 FDA reports)
DEHYDRATION ( 16 FDA reports)
DISTURBANCE IN ATTENTION ( 16 FDA reports)
DYSLIPIDAEMIA ( 16 FDA reports)
HAEMATEMESIS ( 16 FDA reports)
JOINT DISLOCATION ( 16 FDA reports)
MULTI-ORGAN FAILURE ( 16 FDA reports)
PROTHROMBIN TIME PROLONGED ( 16 FDA reports)
TREMOR ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
ABDOMINAL DISTENSION ( 15 FDA reports)
ABNORMAL DREAMS ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 15 FDA reports)
ADRENAL INSUFFICIENCY ( 15 FDA reports)
APPENDICITIS ( 15 FDA reports)
BACTERAEMIA ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
HYPOXIA ( 15 FDA reports)
NEPHROPATHY TOXIC ( 15 FDA reports)
OVERDOSE ( 15 FDA reports)
PAIN IN JAW ( 15 FDA reports)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ( 15 FDA reports)
RASH PAPULAR ( 15 FDA reports)
RENAL TUBULAR DISORDER ( 15 FDA reports)
STEVENS-JOHNSON SYNDROME ( 15 FDA reports)
VIRAL MUTATION IDENTIFIED ( 15 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 14 FDA reports)
MUCOSAL DISCOLOURATION ( 14 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 14 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 14 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 14 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
SWELLING FACE ( 14 FDA reports)
UROSEPSIS ( 14 FDA reports)
ABORTION INDUCED ( 13 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 13 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 13 FDA reports)
GASTRITIS ( 13 FDA reports)
HEPATOTOXICITY ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
LEUKOENCEPHALOPATHY ( 13 FDA reports)
MICROCYTIC ANAEMIA ( 13 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 13 FDA reports)
MYOCARDITIS ( 13 FDA reports)
OXYGEN SATURATION DECREASED ( 13 FDA reports)
PSYCHOTIC DISORDER ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
RHINORRHOEA ( 13 FDA reports)
URINE COLOUR ABNORMAL ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 12 FDA reports)
CUSHING'S SYNDROME ( 12 FDA reports)
DYSGEUSIA ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
PERSISTENT LEFT SUPERIOR VENA CAVA ( 12 FDA reports)
PREMATURE LABOUR ( 12 FDA reports)
PROSTATIC ABSCESS ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
TACHYPNOEA ( 12 FDA reports)
THERAPY NON-RESPONDER ( 12 FDA reports)
VARICES OESOPHAGEAL ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
ANXIETY ( 11 FDA reports)
BLOOD POTASSIUM INCREASED ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
FACIAL WASTING ( 11 FDA reports)
HEPATITIS B ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
HYPOPHOSPHATAEMIA ( 11 FDA reports)
IRON DEFICIENCY ANAEMIA ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
LIPOHYPERTROPHY ( 11 FDA reports)
NECROSIS ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
PORTAL VEIN THROMBOSIS ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
RASH MACULAR ( 11 FDA reports)
RECTAL CANCER ( 11 FDA reports)
SPEECH DISORDER ( 11 FDA reports)
SUBDURAL HAEMATOMA ( 11 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
AFFECT LABILITY ( 10 FDA reports)
ARTHROPOD BITE ( 10 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 10 FDA reports)
FAECES DISCOLOURED ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HEPATIC NECROSIS ( 10 FDA reports)
HEPATOSPLENOMEGALY ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
IMMUNODEFICIENCY ( 10 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 10 FDA reports)
INFLAMMATION ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
INJURY ( 10 FDA reports)
MALARIA ( 10 FDA reports)
METASTASIS ( 10 FDA reports)
MOBILITY DECREASED ( 10 FDA reports)
MUCOUS MEMBRANE DISORDER ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
OSTEOPENIA ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
VIROLOGIC FAILURE ( 10 FDA reports)
APHASIA ( 9 FDA reports)
APHTHOUS STOMATITIS ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 9 FDA reports)
BONE MARROW FAILURE ( 9 FDA reports)
CARDIAC MURMUR ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
DYSPNOEA EXERTIONAL ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
HYPERCHOLESTEROLAEMIA ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
INFECTION ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
MOVEMENT DISORDER ( 9 FDA reports)
MYOSITIS ( 9 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 9 FDA reports)
POLYDACTYLY ( 9 FDA reports)
POLYNEUROPATHY ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
STILLBIRTH ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 8 FDA reports)
BLISTER ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
COMA ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
LIVE BIRTH ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
MOUTH ULCERATION ( 8 FDA reports)
NEUROGENIC BLADDER ( 8 FDA reports)
PROCTALGIA ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
ACIDOSIS ( 7 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 7 FDA reports)
ANION GAP DECREASED ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 7 FDA reports)
BEHCET'S SYNDROME ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
BREATH SOUNDS ABNORMAL ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
EYE DISCHARGE ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HYPOKINESIA ( 7 FDA reports)
HYPOREFLEXIA ( 7 FDA reports)
ILEAL ULCER ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
MALIGNANT HYPERTENSION ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NEONATAL RESPIRATORY ARREST ( 7 FDA reports)
NEUROLOGICAL SYMPTOM ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
OPPORTUNISTIC INFECTION ( 7 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 7 FDA reports)
PSORIASIS ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
SINOATRIAL BLOCK ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ACUTE ABDOMEN ( 6 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRAIN STEM HAEMORRHAGE ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CATARACT ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG PRESCRIBING ERROR ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
OSTEOMALACIA ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SKIN REACTION ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
TONSILLITIS ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
APLASIA ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BRAIN DAMAGE ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CONGENITAL JAW MALFORMATION ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
CUBITAL TUNNEL SYNDROME ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
ENCEPHALITIS VIRAL ( 5 FDA reports)
ENTEROCOCCAL INFECTION ( 5 FDA reports)
FEAR ( 5 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INSULIN RESISTANCE ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
LIVER TRANSPLANT REJECTION ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PATHOGEN RESISTANCE ( 5 FDA reports)
PHARYNGOTONSILLITIS ( 5 FDA reports)
PLAGIOCEPHALY ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
PULMONARY TUBERCULOSIS ( 5 FDA reports)
RENAL TUBULAR ACIDOSIS ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
SUBCUTANEOUS ABSCESS ( 5 FDA reports)
SYNDACTYLY ( 5 FDA reports)
SYPHILIS ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
TRANSFUSION REACTION ( 5 FDA reports)
TREATMENT FAILURE ( 5 FDA reports)
TRISOMY 21 ( 5 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 4 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
ERYTHEMA INFECTIOSUM ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FALL ( 4 FDA reports)
FAT TISSUE INCREASED ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
LIMB MALFORMATION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MITOCHONDRIAL DNA DELETION ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
POLYSUBSTANCE ABUSE ( 4 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETINITIS ( 4 FDA reports)
SCHISTOSOMIASIS ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TARDIVE DYSKINESIA ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
TOXOPLASMOSIS ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR HYPOPLASIA ( 4 FDA reports)
VISCERAL LEISHMANIASIS ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
5'NUCLEOTIDASE INCREASED ( 3 FDA reports)
ABDOMINAL INJURY ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
AIDS RELATED COMPLICATION ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
AMINOACIDURIA ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD IRON INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BLOOD ZINC DECREASED ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CRYING ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CRYSTAL NEPHROPATHY ( 3 FDA reports)
CSF LACTATE INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GIARDIASIS ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HIV INFECTION CDC CATEGORY B3 ( 3 FDA reports)
HIV WASTING SYNDROME ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JAW CYST ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LUNG INJURY ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MASS ( 3 FDA reports)
MEASLES ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 3 FDA reports)
MICROCEPHALY ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NEUROSYPHILIS ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PERIANAL ABSCESS ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PHYSICAL DISABILITY ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PROTEIN S DEFICIENCY ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCAR ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SEX HORMONE BINDING GLOBULIN DECREASED ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TINEA CAPITIS ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
ULCER ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WEIGHT GAIN POOR ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AMOEBIASIS ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOROIDITIS ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
COAGULATION FACTOR VII LEVEL INCREASED ( 2 FDA reports)
COELIAC ARTERY STENOSIS ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FAT ATROPHY ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATITIS B VIRUS ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HOMOCYSTINAEMIA ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
KAPOSI'S SARCOMA AIDS RELATED ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICAL OBSERVATION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MITOCHONDRIAL DNA DEPLETION ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBESITY ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SELECTIVE ABORTION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TUBERCULOID LEPROSY ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VON WILLEBRAND'S DISEASE ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADACTYLY ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENALITIS ( 1 FDA reports)
AIDS DEMENTIA COMPLEX ( 1 FDA reports)
AIDS RETINOPATHY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID ABNORMAL ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASIA CUTIS CONGENITA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL BOWING OF LONG BONES ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOCORTICOIDS INCREASED ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS B DNA INCREASED ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERBAL TOXICITY ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIV ASSOCIATED NEPHROPATHY ( 1 FDA reports)
HIV DISEASE PROGRESSION ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOSTHENURIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACTATE PYRUVATE RATIO INCREASED ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGENIA ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PARTIAL LIPODYSTROPHY ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHIATRIC INVESTIGATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY PERCUSSION TEST ABNORMALITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RICKETS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALIVARY GLAND CYST ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VACCINATION FAILURE ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL HEPATITIS CARRIER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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