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

DRUG INEFFECTIVE ( 14 FDA reports)
PRODUCT QUALITY ISSUE ( 13 FDA reports)
DYSPNOEA ( 12 FDA reports)
HEADACHE ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
BACK PAIN ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
PAIN ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
VOMITING ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TREMOR ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
BREAST ABSCESS ( 4 FDA reports)
BREAST CELLULITIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FALL ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
GALACTORRHOEA ( 4 FDA reports)
GINGIVAL PAIN ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
INTERNAL HERNIA ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DUODENOGASTRIC REFLUX ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MENINGOCOCCAL INFECTION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
AUTISM ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TIC ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH ANKYLOSIS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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