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CONDITION AGGRAVATED ( 8 FDA reports)
PNEUMONIA ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
ALLERGIC CYSTITIS ( 2 FDA reports)
ARRHYTHMIA NEONATAL ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
FALL ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PLATELET AGGREGATION DECREASED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIOULNAR SYNOSTOSIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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