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

ARTHRALGIA ( 18 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
HEADACHE ( 14 FDA reports)
NAUSEA ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
ASTHMA ( 9 FDA reports)
PAIN ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
VOMITING ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
DIZZINESS ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RASH ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COXSACKIE VIRAL INFECTION ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MYOPERICARDITIS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SCAR ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SURGERY ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACNE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THIRST ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)