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

DRUG INEFFECTIVE ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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