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

HEADACHE ( 24 FDA reports)
HYPERTENSION ( 16 FDA reports)
DIARRHOEA ( 15 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
PALPITATIONS ( 13 FDA reports)
DYSPNOEA ( 12 FDA reports)
DIZZINESS ( 11 FDA reports)
FLUSHING ( 11 FDA reports)
INTENTIONAL MISUSE ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
PAIN ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
BRADYCARDIA ( 8 FDA reports)
COUGH ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
BLEEDING TIME ABNORMAL ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
DILATATION VENTRICULAR ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
GALLOP RHYTHM PRESENT ( 7 FDA reports)
GASTRITIS HAEMORRHAGIC ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPOKINESIA ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
PROTEINURIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RALES ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
SPUTUM PURULENT ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ERYTHEMA OF EYELID ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
HYPOGEUSIA ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
NEPHROPATHY TOXIC ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TONGUE DRY ( 6 FDA reports)
VASCULAR RUPTURE ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HYPERTRICHOSIS ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
PARAESTHESIA ORAL ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
AGITATION ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SCAR ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)

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