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

PYREXIA ( 61 FDA reports)
HYPERTENSION ( 59 FDA reports)
WEIGHT INCREASED ( 56 FDA reports)
FEAR OF EATING ( 53 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 52 FDA reports)
RENAL FAILURE ACUTE ( 52 FDA reports)
DEHYDRATION ( 50 FDA reports)
DYSPEPSIA ( 49 FDA reports)
NAUSEA ( 49 FDA reports)
ATRIAL FIBRILLATION ( 47 FDA reports)
BACK PAIN ( 47 FDA reports)
OEDEMA ( 47 FDA reports)
RECTAL HAEMORRHAGE ( 47 FDA reports)
OLIGURIA ( 42 FDA reports)
RENAL PAIN ( 39 FDA reports)
VOMITING ( 39 FDA reports)
CONSTIPATION ( 36 FDA reports)
HAEMORRHOIDS ( 25 FDA reports)
ANAL HAEMORRHAGE ( 17 FDA reports)
RENAL FAILURE ( 17 FDA reports)
DRUG INTERACTION ( 16 FDA reports)
FATIGUE ( 14 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
TOXIC SHOCK SYNDROME ( 11 FDA reports)
DIARRHOEA ( 10 FDA reports)
AGITATION ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
HYPOTENSION ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
TREMOR ( 6 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
ANGER ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FEELINGS OF WORTHLESSNESS ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CAUDAL REGRESSION SYNDROME ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
OBESITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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