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

FATIGUE ( 16 FDA reports)
NAUSEA ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
PAIN ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TIC ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use