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

DRUG INEFFECTIVE ( 21 FDA reports)
CONVULSION ( 18 FDA reports)
DIZZINESS ( 18 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 17 FDA reports)
NAUSEA ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
FATIGUE ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
INJECTION SITE ERYTHEMA ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
ASTHMA ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
DYSPEPSIA ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
RASH ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
EMOTIONAL DISORDER ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PAIN ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RECTAL DISCHARGE ( 7 FDA reports)
SINUS CONGESTION ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 7 FDA reports)
WEIGHT FLUCTUATION ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
AGITATION ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
OBSESSIVE THOUGHTS ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ABASIA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
BITE ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
SCREAMING ( 5 FDA reports)
STARING ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MYCOTIC ALLERGY ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
ADRENAL CYST ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EUSTACHIAN TUBE DISORDER ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJOINED TWINS ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TIC ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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