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

HYPERTENSION ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
APLASIA PURE RED CELL ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
ARTHRITIS ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
BREAST PAIN ( 7 FDA reports)
CERVICOBRACHIAL SYNDROME ( 7 FDA reports)
CHRONIC FATIGUE SYNDROME ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
EPIGASTRIC DISCOMFORT ( 7 FDA reports)
FALL ( 7 FDA reports)
FAT NECROSIS ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
PAIN ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
RADICULITIS BRACHIAL ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
VASCULAR CALCIFICATION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
HYPOTENSION ( 5 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
OVARIAN FAILURE ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SYNOVECTOMY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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