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

BLOOD GLUCOSE INCREASED ( 7 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ULCER ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENSION ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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