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

RENAL FAILURE ( 26 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 24 FDA reports)
CELLULITIS ( 22 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 22 FDA reports)
FEBRILE NEUTROPENIA ( 22 FDA reports)
FUNGAL INFECTION ( 22 FDA reports)
PYREXIA ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
INFECTION ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
RASH ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
IMMUNOGLOBULINS DECREASED ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
NAIL DYSTROPHY ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPILATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
FALL ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEUKODERMA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
PHYSICAL ABUSE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VERBAL ABUSE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
AUTOPHONY ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CYST ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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