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

ABORTION SPONTANEOUS ( 10 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
NERVE ROOT LESION ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
ACNE ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
DEATH ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLITIS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHOLESTASIS OF PREGNANCY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
URETERIC FISTULA ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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