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

NAUSEA ( 19 FDA reports)
DYSPNOEA ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 14 FDA reports)
DIZZINESS ( 12 FDA reports)
VOMITING ( 10 FDA reports)
SYNCOPE ( 9 FDA reports)
COUGH ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
PAIN ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
GOUT ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
MALAISE ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
SWELLING ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DEATH ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
GASTRIC OPERATION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
INJURY ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACNE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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