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

ARTHRALGIA ( 12 FDA reports)
PNEUMONIA ( 9 FDA reports)
NAUSEA ( 8 FDA reports)
PAIN ( 8 FDA reports)
FLUSHING ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
FALL ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RASH ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASTROCYTOMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POISONING ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISTRIBUTION WIDTH ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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