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

DRUG INEFFECTIVE ( 168 FDA reports)
HEADACHE ( 40 FDA reports)
INSOMNIA ( 31 FDA reports)
DYSPNOEA ( 30 FDA reports)
URTICARIA ( 23 FDA reports)
DIZZINESS ( 22 FDA reports)
FATIGUE ( 20 FDA reports)
HYPERSENSITIVITY ( 19 FDA reports)
DRUG EFFECT DECREASED ( 18 FDA reports)
DYSPHAGIA ( 18 FDA reports)
NASAL CONGESTION ( 18 FDA reports)
NAUSEA ( 17 FDA reports)
NASOPHARYNGITIS ( 14 FDA reports)
RASH ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
FEELING JITTERY ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
DIARRHOEA ( 11 FDA reports)
DYSGEUSIA ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
PAIN ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
VOMITING ( 11 FDA reports)
EYE SWELLING ( 10 FDA reports)
LIP SWELLING ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
TREMOR ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
SINUS HEADACHE ( 8 FDA reports)
APHASIA ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
COUGH ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
MALAISE ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SWELLING ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
FALL ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PRODUCT SIZE ISSUE ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
SEDATION ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLISTER ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MYOCARDITIS INFECTIOUS ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
CAPSULE ISSUE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRODUCT BLISTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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