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

DYSPNOEA ( 17 FDA reports)
NAUSEA ( 16 FDA reports)
HEADACHE ( 15 FDA reports)
PNEUMONIA ( 14 FDA reports)
DIARRHOEA ( 12 FDA reports)
VOMITING ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ABNORMAL DREAMS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PAIN ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROCRYPTOCOCCOSIS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM NORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OESTRADIOL DECREASED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SENSORY GANGLIONITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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