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

DYSPNOEA ( 8 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RASH ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND HEALING NORMAL ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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