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

COMPLETED SUICIDE ( 179 FDA reports)
CARDIAC ARREST ( 78 FDA reports)
DYSPNOEA ( 69 FDA reports)
HYPOTENSION ( 67 FDA reports)
RESPIRATORY ARREST ( 61 FDA reports)
PAIN ( 59 FDA reports)
ASTHENIA ( 57 FDA reports)
ARTHRALGIA ( 55 FDA reports)
ANXIETY ( 52 FDA reports)
NAUSEA ( 49 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 47 FDA reports)
MULTIPLE DRUG OVERDOSE ( 47 FDA reports)
DIARRHOEA ( 46 FDA reports)
HEADACHE ( 46 FDA reports)
PAIN IN EXTREMITY ( 46 FDA reports)
PYREXIA ( 46 FDA reports)
DEATH ( 45 FDA reports)
RENAL FAILURE ACUTE ( 45 FDA reports)
DRUG INTERACTION ( 44 FDA reports)
VOMITING ( 41 FDA reports)
WEIGHT DECREASED ( 40 FDA reports)
ANAEMIA ( 39 FDA reports)
DIZZINESS ( 39 FDA reports)
DEEP VEIN THROMBOSIS ( 38 FDA reports)
BACK PAIN ( 37 FDA reports)
FALL ( 37 FDA reports)
PRURITUS ( 37 FDA reports)
LOSS OF CONSCIOUSNESS ( 36 FDA reports)
MALAISE ( 36 FDA reports)
CHEST PAIN ( 34 FDA reports)
CONFUSIONAL STATE ( 33 FDA reports)
PULMONARY EMBOLISM ( 33 FDA reports)
FATIGUE ( 32 FDA reports)
OEDEMA PERIPHERAL ( 32 FDA reports)
COUGH ( 31 FDA reports)
DEPRESSION ( 31 FDA reports)
ABDOMINAL PAIN ( 29 FDA reports)
CHOLELITHIASIS ( 29 FDA reports)
HYPONATRAEMIA ( 29 FDA reports)
RASH ( 29 FDA reports)
CARDIO-RESPIRATORY ARREST ( 28 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 28 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 28 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 26 FDA reports)
CONSTIPATION ( 26 FDA reports)
DEHYDRATION ( 26 FDA reports)
PNEUMONIA ( 26 FDA reports)
POISONING ( 26 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
CHOLESTASIS ( 24 FDA reports)
DYSPHAGIA ( 24 FDA reports)
EPISTAXIS ( 24 FDA reports)
HYPERHIDROSIS ( 24 FDA reports)
INTENTIONAL DRUG MISUSE ( 24 FDA reports)
INTESTINAL OBSTRUCTION ( 24 FDA reports)
MYOCARDIAL INFARCTION ( 24 FDA reports)
PULMONARY OEDEMA ( 24 FDA reports)
SOMNOLENCE ( 24 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 23 FDA reports)
DRUG TOXICITY ( 23 FDA reports)
OVERDOSE ( 23 FDA reports)
PLEURAL EFFUSION ( 23 FDA reports)
ERYTHEMA ( 22 FDA reports)
MYALGIA ( 22 FDA reports)
PALPITATIONS ( 22 FDA reports)
SYNCOPE ( 22 FDA reports)
TACHYCARDIA ( 22 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 22 FDA reports)
URINARY TRACT INFECTION ( 22 FDA reports)
CHOLECYSTITIS CHRONIC ( 21 FDA reports)
CROHN'S DISEASE ( 21 FDA reports)
MITRAL VALVE INCOMPETENCE ( 21 FDA reports)
HYPERTENSION ( 20 FDA reports)
RESPIRATORY FAILURE ( 20 FDA reports)
SUICIDAL IDEATION ( 20 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
DISORIENTATION ( 19 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 19 FDA reports)
TREMOR ( 19 FDA reports)
VERTIGO ( 19 FDA reports)
DIPLOPIA ( 18 FDA reports)
DRY MOUTH ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
HYPOGLYCAEMIA ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
THROMBOSIS ( 18 FDA reports)
COLITIS ( 17 FDA reports)
CYTOLYTIC HEPATITIS ( 17 FDA reports)
DEPENDENCE ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
HAEMATOMA ( 17 FDA reports)
RENAL FAILURE ( 17 FDA reports)
RHEUMATOID ARTHRITIS ( 17 FDA reports)
SEPSIS ( 17 FDA reports)
STRESS ( 17 FDA reports)
VISUAL IMPAIRMENT ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
BLINDNESS ( 16 FDA reports)
BONE PAIN ( 16 FDA reports)
CHROMATURIA ( 16 FDA reports)
CYST ( 16 FDA reports)
DYSURIA ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
HYPOXIA ( 16 FDA reports)
INFLUENZA LIKE ILLNESS ( 16 FDA reports)
SKIN DISCOLOURATION ( 16 FDA reports)
ABDOMINAL DISTENSION ( 15 FDA reports)
ARRHYTHMIA ( 15 FDA reports)
BRADYCARDIA ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
CARDIAC DISORDER ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
CERVICAL DYSPLASIA ( 15 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
FRACTURE ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
HIP FRACTURE ( 15 FDA reports)
HYPERTHERMIA ( 15 FDA reports)
ILEITIS ( 15 FDA reports)
IRRITABLE BOWEL SYNDROME ( 15 FDA reports)
LYMPHADENOPATHY ( 15 FDA reports)
PROTEINURIA ( 15 FDA reports)
UNRESPONSIVE TO STIMULI ( 15 FDA reports)
ACNE ( 14 FDA reports)
AORTIC VALVE INCOMPETENCE ( 14 FDA reports)
ASCITES ( 14 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
COLITIS ULCERATIVE ( 14 FDA reports)
DEVICE RELATED INFECTION ( 14 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 14 FDA reports)
LIP DRY ( 14 FDA reports)
MOUTH ULCERATION ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
NOCTURIA ( 14 FDA reports)
PAIN IN JAW ( 14 FDA reports)
POLLAKIURIA ( 14 FDA reports)
PULMONARY HYPERTENSION ( 14 FDA reports)
SINUSITIS ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
ACCIDENTAL EXPOSURE ( 13 FDA reports)
ANOREXIA ( 13 FDA reports)
BALANCE DISORDER ( 13 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CATARACT ( 13 FDA reports)
DRY EYE ( 13 FDA reports)
FACIAL PAIN ( 13 FDA reports)
FLUSHING ( 13 FDA reports)
GLOSSITIS ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 13 FDA reports)
MYOCARDIAL ISCHAEMIA ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
STITCH ABSCESS ( 13 FDA reports)
TOOTHACHE ( 13 FDA reports)
ALOPECIA ( 12 FDA reports)
AMAUROSIS FUGAX ( 12 FDA reports)
ATROPHIC VULVOVAGINITIS ( 12 FDA reports)
BACK DISORDER ( 12 FDA reports)
BONE DISORDER ( 12 FDA reports)
BRUXISM ( 12 FDA reports)
CARDIOGENIC SHOCK ( 12 FDA reports)
CARDIOMEGALY ( 12 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 12 FDA reports)
DECREASED INTEREST ( 12 FDA reports)
ENDOTRACHEAL INTUBATION ( 12 FDA reports)
EYE IRRITATION ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
HYPOAESTHESIA ORAL ( 12 FDA reports)
INFLAMMATION ( 12 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 12 FDA reports)
IRIS ADHESIONS ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
METASTASES TO LIVER ( 12 FDA reports)
NECK PAIN ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
SWOLLEN TONGUE ( 12 FDA reports)
TONGUE ULCERATION ( 12 FDA reports)
TOXIC SKIN ERUPTION ( 12 FDA reports)
ACIDOSIS ( 11 FDA reports)
AGITATION ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
BRAIN OEDEMA ( 11 FDA reports)
COMA ( 11 FDA reports)
CONTUSION ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
ECZEMA ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
HAEMATURIA ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HEPATIC LESION ( 11 FDA reports)
HEPATOMEGALY ( 11 FDA reports)
INFECTION ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
MOBILITY DECREASED ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
RASH MACULO-PAPULAR ( 11 FDA reports)
RHABDOMYOLYSIS ( 11 FDA reports)
AZOTAEMIA ( 10 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
OLIGURIA ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
TRICUSPID VALVE DISEASE ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
AMNESIA ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CARDIAC OUTPUT DECREASED ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
GANGRENE ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
SERRATIA BACTERAEMIA ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
SWELLING ( 9 FDA reports)
VENTRICULAR FIBRILLATION ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
ARTHROPATHY ( 8 FDA reports)
CARDIOMYOPATHY ( 8 FDA reports)
CSF GLUCOSE DECREASED ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
EJECTION FRACTION DECREASED ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE PAIN ( 8 FDA reports)
MELAENA ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
SKIN WARM ( 8 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 8 FDA reports)
VARICOSE VEIN ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ARTHRITIS ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EYE PAIN ( 7 FDA reports)
FAECES DISCOLOURED ( 7 FDA reports)
FEAR ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
INJURY ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LEUKOCYTOSIS ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
SINUS OPERATION ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SUBILEUS ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
ARTHRITIS BACTERIAL ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CATARACT OPERATION ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CONVERSION DISORDER ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DRUG ABUSER ( 6 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
IMPAIRED DRIVING ABILITY ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
MASS ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
NECROSIS ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PHLEBITIS ( 6 FDA reports)
PURPURA ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
SHOULDER PAIN ( 6 FDA reports)
TOOTH REPAIR ( 6 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CARDIORENAL SYNDROME ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
INAPPROPRIATE AFFECT ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
POST THROMBOTIC SYNDROME ( 5 FDA reports)
POSTOPERATIVE ILEUS ( 5 FDA reports)
RALES ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
TENSION ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MACULAR CYST ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
POUCHITIS ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONGENITAL NOSE MALFORMATION ( 3 FDA reports)
CRYING ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FACIAL DYSMORPHISM ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FISTULA ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MICROGNATHIA ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
NASAL CAVITY PACKING ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OESOPHAGEAL ATRESIA ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORTHOSTATIC INTOLERANCE ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RETROGNATHIA ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VITREOUS DETACHMENT ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL JAW MALFORMATION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MONONUCLEOSIS SYNDROME ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCAR ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
AMMONIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLEDOCHAL CYST ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUTTERING ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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