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

RENAL FAILURE ( 18 FDA reports)
ANXIETY ( 13 FDA reports)
DIARRHOEA ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
FATIGUE ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
AGGRESSION ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH ( 3 FDA reports)
SEDATION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EHLERS-DANLOS SYNDROME ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYSTITIS-LIKE SYMPTOM ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TIC ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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