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

PYREXIA ( 74 FDA reports)
INTERSTITIAL LUNG DISEASE ( 61 FDA reports)
RASH ( 51 FDA reports)
PNEUMONIA ( 49 FDA reports)
LIVER DISORDER ( 40 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 37 FDA reports)
INJECTION SITE PAIN ( 28 FDA reports)
CONDITION AGGRAVATED ( 26 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 26 FDA reports)
PANCYTOPENIA ( 26 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 25 FDA reports)
ERYTHEMA ( 24 FDA reports)
RHEUMATOID ARTHRITIS ( 24 FDA reports)
ARTHRALGIA ( 23 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
MALAISE ( 22 FDA reports)
NAUSEA ( 22 FDA reports)
HEADACHE ( 21 FDA reports)
INJECTION SITE ERYTHEMA ( 21 FDA reports)
PLATELET COUNT DECREASED ( 20 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
INFUSION RELATED REACTION ( 19 FDA reports)
PAIN ( 19 FDA reports)
DYSPNOEA ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
DIZZINESS ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
DIARRHOEA ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 14 FDA reports)
DRUG ERUPTION ( 14 FDA reports)
VOMITING ( 14 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
PULMONARY TUBERCULOSIS ( 13 FDA reports)
INJECTION SITE PRURITUS ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CHILLS ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
LYMPHADENOPATHY ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
SHOCK ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 10 FDA reports)
RASH GENERALISED ( 10 FDA reports)
COUGH ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 9 FDA reports)
DISSEMINATED TUBERCULOSIS ( 9 FDA reports)
ECZEMA ( 9 FDA reports)
FEMUR FRACTURE ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
BONE MARROW FAILURE ( 8 FDA reports)
INFECTION ( 8 FDA reports)
NEPHROTIC SYNDROME ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
BRONCHITIS ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
EXANTHEM ( 7 FDA reports)
FACE OEDEMA ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
GENERALISED ERYTHEMA ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
IGA NEPHROPATHY ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INJECTION SITE RASH ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
CELLULITIS ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
FALL ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
INJECTION SITE IRRITATION ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 6 FDA reports)
MELAENA ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
TUBERCULOUS PLEURISY ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DEATH ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROINTESTINAL PERFORATION ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
PLEURISY ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
TREMOR ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ANURIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CATARACT ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HYPERVIGILANCE ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PYOTHORAX ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SEDATION ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPH NODE TUBERCULOSIS ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MEASLES ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
ROTATOR CUFF REPAIR ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STRESS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEURILEMMOMA BENIGN ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL FIBROMA ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR NEOPLASM ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLAVOBACTERIUM INFECTION ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
HAEMANGIOMA CONGENITAL ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALIGNANT LYMPHOID NEOPLASM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODULE ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONONUCLEOSIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR GERM CELL CANCER ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VERTEBRAL ABSCESS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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