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

DYSPNOEA ( 8 FDA reports)
NAUSEA ( 6 FDA reports)
CONSTIPATION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
FALL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TENSION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)

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