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

ANAPHYLACTIC REACTION ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ASTHMA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
COUGH ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
MELAENA ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE PIGMENTATION CHANGES ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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