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

DIZZINESS ( 9 FDA reports)
BICYTOPENIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DEATH ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BUNION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)

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