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

DIARRHOEA ( 36 FDA reports)
PRURITUS ( 27 FDA reports)
FATIGUE ( 21 FDA reports)
PYREXIA ( 21 FDA reports)
VOMITING ( 19 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
CHOLESTASIS ( 16 FDA reports)
DEHYDRATION ( 16 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
RASH ( 15 FDA reports)
ANOREXIA ( 14 FDA reports)
DIZZINESS ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
JAUNDICE ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
CONSTIPATION ( 12 FDA reports)
LUNG DISORDER ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
HYPOTENSION ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HEPATITIS CHOLESTATIC ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
FALL ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
COMA ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
COUGH ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
DEATH ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
PAIN ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXTREMITY CONTRACTURE ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MUTISM ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 4 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PERINEAL ABSCESS ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
INFECTION ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PELVIC INFECTION ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENEMA ADMINISTRATION ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
STROKE VOLUME DECREASED ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
ANAL POLYP ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL DISCOMFORT ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
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PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
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RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROSTERNAL INFECTION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
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SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)

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